Cas no 92136-39-5 (Boc-Propargylamine)

Boc-Propargylamine structure

Product Name:Boc-Propargylamine

CAS No:92136-39-5

MF:C₈H₁₃NO₂

MW:155.194322347641

MDL:MFCD07367245

CID:61547

PubChem ID:253662096

Update Time:2024-10-26

Boc-Propargylamine Chemical and Physical Properties

Names and Identifiers

- N-Boc-Propargylamine
- N-(tert-Butoxycarbonyl)propargyl amine
- N-Boc-Prop-2-ynylaMine
- N-Boc-Propaylamine
- tert-butyl N-prop-2-ynylcarbamate
- tert-Butyl 2-Propynylcarbamate
- 2-Propynylcarbamic Acid tert-Butyl Ester
- 1,1-Dimethylethyl N-2-propyn-1-ylcarbamate (ACI)
- Carbamic acid, 2-propynyl-, 1,1-dimethylethyl ester (9CI)
- 1,1-Dimethylethyl 2-propyn-1-ylcarbamate
- 3-(tert-Butoxycarbonylamino)prop-1-yne
- 3-[(tert-Butyloxycarbonyl)amino]-1-propyne
- Boc-propargylamine
- N-(Prop-2-ynyl)carbamic acid tert-butyl ester
- N-(tert-Butoxycarbonyl)propargylamine
- N-tert-Butoxycarbonyl-2-propyn-1-amine
- tert-Butyl (2-propyn-1-yl)carbamate
- tert-Butyl N-(2-propyn-1-yl)carbamate
- tert-Butyl N-propargylcarbamate
- tert-Butyl propargylcarbamate
- 3-t-butoxycarbonylamino-1-propyne
- N-(t-butoxycarbonyl)-propargylamine
- DTXSID10454171
- ALBB-028033
- N-t-butoxycarbonyl propargylamine
- SY025866
- t-Butyloxycarbonyl Propargyl Amine
- AKOS005068276
- N-2-Propyn-1-yl-carbamic Acid 1,1-Dimethylethyl Ester;
- t-butoxycarbonylpropargylamine
- B4472
- n-(tert-butyloxycarbonyl)propargylamine
- 92136-39-5
- tert-butyl N-(prop-2-yn-1-yl)carbamate
- N-tert-butoxycarbonylpropargylamine
- MFCD07367245
- Z804942822
- 3-(t-butoxycarbonylamino) propyne
- t-Butyl N-(2-propynyl)carbamate
- t-butyl propargylcarbamate
- tert-butyl prop-2-yn-1-ylcarbamate
- prop-2-ynyl-carbamic acid tert-butyl ester
- N-tert.-butoxycarbonyl-prop-2-ynylamine
- N-Boc propargylamine
- EN300-54075
- SCHEMBL16913
- t-butyl prop-2-ynylcarbamate
- TERT-BUTYL PROP-2-YNYLCARBAMATE
- AB31117
- N-(Tert-Butoxycarbonyl)propargylamne
- CARBAMIC ACID, 2-PROPYNYL-, 1,1-DIMETHYLETHYL ESTER
- SS-3353
- (2-propynyl)carbamic acid tert-butyl ester
- HY-75970
- TERT-BUTYL N-(2-PROPYNYL)CARBAMATE
- CS-M0556
- N-Boc-propargylamine, 97%
- Prop-2-ynyl-carbamic acid t-butyl ester
- propargyl Boc-amine
- n-boc propargyl amine
- N-(Boc)-propargylamine
- J-523185
- N-t-butoxycarbonylpropargylamine
- N-Boc-2-propyn-1-amine
- (Boc)Propargylamin
- N-tert-butoxycarbonyl-propargylamine
- n-boc-propargyl amine
- Boc-Propargylamine
- MDL： MFCD07367245
- Inchi： 1S/C8H13NO2/c1-5-6-9-7(10)11-8(2,3)4/h1H,6H2,2-4H3,(H,9,10)
- InChI Key： DSPYCWLYGXGJNJ-UHFFFAOYSA-N
- SMILES： O=C(NCC#C)OC(C)(C)C

Computed Properties

Exact Mass: 155.09500
Monoisotopic Mass: 155.094628657g/mol
Isotope Atom Count: 0
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 3
Heavy Atom Count: 11
Rotatable Bond Count: 4
Complexity: 182
Covalently-Bonded Unit Count: 1
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count : 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
XLogP3: 1
Topological Polar Surface Area: 38.3?2

Experimental Properties

Melting Point: 40.0 to 44.0 deg-C
Boiling Point: 170°C/14mmHg(lit.)
Flash Point: Fahrenheit: 199.4 ° f < br / > Celsius: 93 ° C < br / >
Solubility: Soluble in chloroform.
PSA: 41.82000
LogP: 1.34870
Sensitiveness: Moisture Sensitive

Boc-Propargylamine Security Information

Symbol:
Prompt：warning
Signal Word：Warning
Hazard Statement： H315-H319
Warning Statement： P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Hazardous Material transportation number：NONH for all modes of transport
WGK Germany：3
Hazard Category Code： 22-36/37/38
Safety Instruction： S26; S36/37; S61
Hazardous Material Identification：
Storage Condition：0-10°C
Risk Phrases：R22; R36/37/38; R52/53

Boc-Propargylamine Customs Data

HS CODE：2924199090
Customs Data：

China Customs Code:
2924199090

Overview:

2924199090. Other acyclic amides(Including acyclic carbamates)(Including its derivatives and salts). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

Declaration elements:

Product Name, component content, use to, packing

Summary:

2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Boc-Propargylamine Pricemore >>

Related Categories	No.	Product Name	Cas No.	Purity	Specification	Price	update time
XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd.	687146-5G	Boc-Propargylamine	92136-39-5		5g	￥931.54	2023-11-29
SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd.	N836841-100g	N-Boc-propargylamine	92136-39-5	97%	100g	1,436.40	2021-05-17
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TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd.	B4472-5G	N-(tert-Butoxycarbonyl)propargylamine	92136-39-5	>98.0%(GC)	5g	￥590.00	2024-04-15
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Boc-Propargylamine Production Method

Production Method 1

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Solvents: Tetrahydrofuran ; 1 h, 75 °C

Reference

: Novel Method of Tetramic Acid Synthesis: Silver-Catalyzed Carbon Dioxide Incorporation into Propargylic Amine and Intramolecular Rearrangement

Ishida, Tomonobu; Kobayashi, Ryo; Yamada, Tohru, Organic Letters, 2014, 16(9), 2430-2433

Production Method 2

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Solvents: Ethyl acetate ; 0 °C → rt; overnight, rt

Reference

: Synthesis of G-quadruplex-targeting flexible macrocyclic molecules via click reactions

Zhang, Qiang; Tan, Wei; Yuan, Gu, ARKIVOC (Gainesville, 2013, (4), 334-345

Production Method 3

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Solvents: Dichloromethane ; 0 °C → rt

Reference

: The Vinyl Moiety as a Handle for Regiocontrol in the Preparation of Unsymmetrical 2,3-Aliphatic-Substituted Indoles and Pyrroles

Huestis, Malcolm P.; Chan, Lina; Stuart, David R.; Fagnou, Keith, Angewandte Chemie, 2011, 50(6), 1338-1341

Production Method 4

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Solvents: Dichloromethane ; 0 °C; 30 min, rt

Reference

: Selective Fluoromethyl Couplings of Alkynes via Nickel Catalysis

Li, Huan; Wang, Fang; Zhu, Shengqing; Chu, Lingling, Angewandte Chemie, 2022, 61(9),

Production Method 5

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Solvents: Dichloromethane ; 25 min, 0 °C; 30 min, rt

Reference

: Preparation of nicotine-related compounds as modulators of smoking or nicotine ingestion and lung cancer

, World Intellectual Property Organization, , ,

Production Method 6

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Solvents: Dichloromethane ; 25 min, 0 °C; 30 min, rt

Reference

: 5-Substituted, 6-Substituted, and Unsubstituted 3-Heteroaromatic Pyridine Analogues of Nicotine as Selective Inhibitors of Cytochrome P-450 2A6

Denton, Travis T.; Zhang, Xiaodong; Cashman, John R., Journal of Medicinal Chemistry, 2005, 48(1), 224-239

Production Method 7

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Solvents: Dichloromethane ; overnight, rt
1.2 Reagents: Sodium chloride ; rt

Reference

: Dual catalytic enantioselective desymmetrization of allene-tethered cyclohexanones

Zhang, Lin; Yamazaki, Ken; Leitch, Jamie A.; Manzano, Ruben; Atkinson, Victoria A. M.; et al, Chemical Science, 2020, 11(28), 7444-7450

Production Method 8

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Solvents: Tetrahydrofuran ; 4 h, 21 °C

Reference

: A pH-Switchable Aqueous Organocatalysis with Amphiphilic Secondary Amine-Porphyrin Hybrids

Arlegui, Aitor; Torres, Pol; Cuesta, Victor; Crusats, Joaquim ; Moyano, Albert, European Journal of Organic Chemistry, 2020, 2020(28), 4399-4407

Production Method 9

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Reagents: Triethylamine Solvents: Dichloromethane ; 18 h, rt

Reference

: Design and synthesis of a peptide derivative of ametantrone targeting the major groove of the d(GGCGCC)2 palindromic sequence

Ongaro, Alberto; Ribaudo, Giovanni; Braud, Emmanuelle; Etheve-Quelquejeu, Melanie; De Franco, Michele; et al, New Journal of Chemistry, 2020, 44(9), 3624-3631

Production Method 10

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

Reference

: The Alkyne Moiety as a Latent Electrophile in Irreversible Covalent Small Molecule Inhibitors of Cathepsin K

Mons, Elma ; Jansen, Ineke D. C.; Loboda, Jure; van Doodewaerd, Bjorn R.; Hermans, Jill; et al, Journal of the American Chemical Society, 2019, 141(8), 3507-3514

Production Method 11

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Solvents: Dichloromethane ; 0 °C; 1 h, rt

Reference

: Achiral Cyclopentadienone Iron Tricarbonyl Complexes Embedded in Streptavidin: An Access to Artificial Iron Hydrogenases and Application in Asymmetric Hydrogenation

Merel, Delphine S.; Gaillard, Sylvain; Ward, Thomas R.; Renaud, Jean-Luc, Catalysis Letters, 2016, 146(3), 564-569

Production Method 12

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Catalysts: 4-(Dimethylamino)pyridine Solvents: Dichloromethane ; 0 °C; 0 °C → rt; 2 h, rt

Reference

: Electrophile-Mediated Reactions of Functionalized Propargylic Substrates

Urbanaite, Aurelija; Jonusis, Mantas; Buksnaitiene, Rita; Balkaitis, Simonas; Cikotiene, Inga, European Journal of Organic Chemistry, 2015, 2015(32), 7091-7113

Production Method 13

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Solvents: Dichloromethane ; 0 °C; 1 h, 0 °C

Reference

: Synthesis of the stereogenic triad of the halicyclamine A core

Molander, Gary A.; Cadoret, Frederic, Tetrahedron Letters, 2011, 52(17), 2199-2202

Production Method 14

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Solvents: Ethyl acetate ; cooled; overnight, rt

Reference

: Flexible lactam macrocyclic molecule useful in treatment of cancer and its preparation

, China, , ,

Production Method 15

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Reagents: Diisopropylamine Solvents: Tetrahydrofuran ; overnight, rt

Reference

: Phenylethynyl-benzamide compounds as glucokinase activators and methods for the preparation thereof

, Korea, , ,

Production Method 16

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Reagents: Triethylamine Solvents: Dichloromethane ; 10 °C; 2 h, 25 °C
1.2 Reagents: Water

Reference

: Hydrogen Bonding-directed Sequential 1,6/1,4-Addition of Heteroatom Nucleophiles onto Electron-deficient 1,3-Diynes

Liyanage Perera, Erandi; Lee, Daesung, Organic Chemistry Frontiers, 2023, 10(1), 209-215

Production Method 17

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Solvents: Dichloromethane ; 0 °C; 30 min, rt

Reference

: Synthesis of 1,2,3-Substituted Pyrroles from Propargylamines via a One-Pot Tandem Enyne Cross Metathesis-Cyclization Reaction

Chachignon, Helene; Scalacci, Nicolo; Petricci, Elena; Castagnolo, Daniele, Journal of Organic Chemistry, 2015, 80(10), 5287-5295

Production Method 18

2450-71-7

24424-99-5

92136-39-5

Reaction Conditions

1.1 Solvents: Tetrahydrofuran ; 0 °C; 0 °C → rt; 2 h, rt

Reference

: Direct Asymmetric α-C-H Addition of N-unprotected Propargylic Amines to Trifluoromethyl Ketones by Carbonyl Catalysis

Ji, Pengwei; Liu, Xiaopei; Xu, Jiwei; Zhang, Xu; Guo, Jianhua; et al, Angewandte Chemie, 2022, 61(48),

Boc-Propargylamine Raw materials

Boc-Propargylamine Preparation Products

Boc-Propargylamine (92136-39-5)

Boc-Propargylamine Suppliers

Amadis Chemical Company Limited

Gold Member

Audited Supplier

(CAS:92136-39-5)Boc-Propargylamine

Order Number:A844153

Stock Status:in Stock

Quantity:500g

Purity:99%

Pricing Information Last Updated:Friday, 30 August 2024 07:02

Price ($):409.0

Email:[email protected]

Product Official Link

Tiancheng Chemical (Jiangsu) Co., Ltd

Gold Member

Audited Supplier

(CAS:92136-39-5)N-Boc-氨基丙炔; N-叔丁氧羰基氨基丙炔

Order Number:LE26827065

Stock Status:in Stock

Quantity:25KG,200KG,1000KG

Purity:99%

Pricing Information Last Updated:Friday, 20 June 2025 12:59

Price ($):discuss personally

Email:[email protected]

Boc-Propargylamine Related Literature

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M. Zeiger,N. J?ckel,P. Strubel,L. Borchardt,R. Reinhold,W. Nickel,J. Eckert,V. Presser,S. Kaskel J. Mater. Chem. A, 2015,3, 17983-17990
2. Excited state dynamics of symmetric and asymmetric Cr3(dpa)4Cl2 measured using femtosecond transient absorption spectroscopy?

Chao-Han Cheng,Wen-Zhen Wang,Shie-Ming Peng,I-Chia Chen Phys. Chem. Chem. Phys., 2017,19, 25471-25477
3. Fate of single walled carbon nanotubes in wetland ecosystems?

Joseph H. Bisesi,Tara Sabo-Attwood Environ. Sci.: Nano, 2014,1, 574-583
4. Evidence of CO2 molecule acting as an electron acceptor on a nanoporous metal–organic-framework MIL-53 or Cr3+(OH)(O2C–C6H4–CO2)?

Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
5. Estimates of hydride ion stability in condensed systems: energy of formation and solvation in aqueous and polar-organic solvents

Craig A. Kelly,David R. Rosseinsky Phys. Chem. Chem. Phys., 2001,3, 2086-2090

Related Categories

Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues Amino acids and derivatives

92136-39-5 (Boc-Propargylamine) Related Products

Recommended suppliers

Amadis Chemical Company Limited

(CAS:92136-39-5)Boc-Propargylamine

Purity:99%

Quantity:500g

Price ($):409.0

Tiancheng Chemical (Jiangsu) Co., Ltd

(CAS:92136-39-5)N-Boc-氨基丙炔; N-叔丁氧羰基氨基丙炔

Purity:99%

Quantity:25KG,200KG,1000KG

Price ($):Inquiry

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Cas no 92136-39-5 (Boc-Propargylamine)

Boc-Propargylamine Chemical and Physical Properties

Names and Identifiers

Computed Properties

Experimental Properties

Boc-Propargylamine Security Information

Boc-Propargylamine Customs Data

China Customs Code:

Overview:

Declaration elements:

Summary:

Boc-Propargylamine Pricemore >>

Boc-Propargylamine Production Method

Production Method 1

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Production Method 18

Boc-Propargylamine Raw materials

Boc-Propargylamine Preparation Products

Boc-Propargylamine Suppliers

Boc-Propargylamine Related Literature

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92136-39-5 (Boc-Propargylamine) Related Products