Cas no 68076-36-8 (NH2-C4-NH-Boc)
NH2-C4-NH-Boc Chemical and Physical Properties
Names and Identifiers
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- tert-Butyl (4-aminobutyl)carbamate
- N-(4-Aminobutyl)carbamic acid tert-butyl ester
- N-Boc-1,4-butanediamine
- N-(tert-Butoxycarbonyl)-1,4-diaminobutane
- 1-Boc-Amino-1,4-butanediamine
- 4-Aminobutylcarbamic Acid tert-Butyl Ester
- Carbamic acid, N-(4-aminobutyl)-, 1,1-dimethylethyl ester
- tert-butyl 4-amino butylcarbamate
- tert-Butyl N-(4-aminobutyl)carbamate
- (4-aminobutyl)carbamic acid 1,1-dimethylethyl ester
- (4-amino-butyl)-carbamic acid tert-butyl ester
- AURORA KA-4397
- BOC-DAB HCL
- BOC-DIAMINOBUTANE HCL
- BOC-NH(CH2)4NH2 HCL
- BUTTPARK 121 6-09
- N-(1,1-dimethylethoxycarbonyl)-1,4-butanediamine
- N-(tert-butoxycarbonyl)-1,4-diamino-butane
- N-Boc-1,4-butandiamine
- N-T-BOC-BUTANDIAMINE HCL
- N-tert-Butoxy
- RARECHEM AR PA 0023
- N-Boc-1,4-diaminobutane
- N-(tert-Butoxycarbonyl)-1,4-butanediamine
- tert-butyl 4-aminobutylcarbamate
- BOC-1,4-DIAMINOBUTANE
- mono-4-N-Boc-1,4-diaminobutane
- N-(4-aminobutyl)carbamic acid t-butyl ester
- Carbamic acid, (4-aminobutyl)-, 1,1-dimethylethyl ester
- N-BOC-1,4-butane
- NH2-C4-NH-Boc
- N-1-Boc-1,4-diaminobutane . HCl
- N-(4-aminobutyl)-carbamic acid t-butyl ester
- N-Boc-1,4-butanediamine, >=97.0% (GC/NT)
- 4-t-butoxycarbonylamino-butylamine
- N-t-butyloxycarbonyl-1,4-diaminobutane
- N-Boc-putrescine
- HY-40178
- 1,1-dimethylethyl (4-aminobutyl)carbamate
- EN300-125900
- A9081
- t-butyl 4-aminobutylcarbamate
- N-Boc-butane-1,4-diamine
- (4-aminobutyl)-carbamic acid t-butyl ester
- A1373
- Q-101918
- MFCD00210019
- (4-aminobutyl)-carbamic acid tert-butyl ester
- t-butyl 4-amino-butylcarbamate
- SCHEMBL181700
- (4-amino-butyl)-carbamic acid t-butyl ester
- 68076-36-8
- AM804224
- FT-0649783
- tert-butyl(4-aminobutyl)carbamate
- ZFQWJXFJJZUVPI-UHFFFAOYSA-N
- n-tert-butyloxycarbonyl-1,4-diaminobutane
- tert-butyl 4-aminobutylaminocarboxylate
- H2N(CH2)4NHBoc
- tert-butyl-N-(4-aminobutyl)carbamate
- AC-2382
- N-(tert-butoxycarbonyl)-1,4-diamino butane
- (4-amino-butyl)carbamic acid tert-butyl ester
- CHEMBL3356838
- GS-5840
- N-tert.-butoxycarbonyl-1,4-diaminobutane
- AKOS005146189
- BP-14003
- CS-D0144
- SY003980
- tert-butyl N-(4-aminobutyl)carbamate,hydrochloride
- BBL101371
- STL555167
- N-(4-Aminobutyl)carbamic Acid 1,1-Dimethylethyl Ester
- DB-030404
-
- MDL： MFCD00210019
- Inchi： 1S/C9H20N2O2/c1-9(2,3)13-8(12)11-7-5-4-6-10/h4-7,10H2,1-3H3,(H,11,12)
- InChI Key： ZFQWJXFJJZUVPI-UHFFFAOYSA-N
- SMILES： O(C(NCCCCN)=O)C(C)(C)C
Computed Properties
- Exact Mass: 188.15200
- Monoisotopic Mass: 188.152
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 13
- Rotatable Bond Count: 6
- Complexity: 152
- 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
- Surface Charge: 0
- Tautomer Count: 2
- XLogP3: 0.7
- Topological Polar Surface Area: 64.4
Experimental Properties
- Color/Form: Clear liquid.
- Density: 0.984?g/mL?at 20?°C(lit.)
- Melting Point: No data available
- Boiling Point: 292.8℃ at 760 mmHg
- Flash Point: Degrees Fahrenheit:228.2°F
Degrees Celsius:109°C - Refractive Index: n20/D 1.460
- PSA: 64.35000
- LogP: 2.34120
- Solubility: Not determined
NH2-C4-NH-Boc Security Information
-
Symbol:
- Prompt：warning
- Signal Word：Danger
- Hazard Statement： H314
- Warning Statement： P280,P305+P351+P338,P310
- Hazardous Material transportation number：UN 2735 8/PG 3
- WGK Germany：3
- Hazard Category Code： 34
- Safety Instruction： S26-S36/37/39-S45
- FLUKA BRAND F CODES：10-34
-
Hazardous Material Identification：
- HazardClass：8
- PackingGroup：III
- Storage Condition：Store at room temperature
- Risk Phrases：R34
NH2-C4-NH-Boc Customs Data
- HS CODE：2924199090
- Customs Data：
China Customs Code:
2924199090Overview:
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%
NH2-C4-NH-Boc Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | 15404-1ML |
NH2-C4-NH-Boc |
68076-36-8 | 1ml |
￥899.71 | 2023-12-10 | ||
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | 15404-5ML |
NH2-C4-NH-Boc |
68076-36-8 | 5ml |
￥3334.13 | 2023-12-10 | ||
| CHENG DOU FEI BO YI YAO Technology Co., Ltd. | ARK-09353-100g |
TERT-BUTYL (4-AMINOBUTYL)CARBAMATE |
68076-36-8 | 97% | 100g |
$374 | 2023-09-07 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | A-DR420-1g |
NH2-C4-NH-Boc |
68076-36-8 | 98% | 1g |
78CNY | 2021-05-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | A-DR420-5g |
NH2-C4-NH-Boc |
68076-36-8 | 98% | 5g |
205CNY | 2021-05-10 | |
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | N802045-25g |
N-Boc-1,4-butanediamine |
68076-36-8 | 95% | 25g |
￥600.00 | 2022-09-01 | |
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | A1373-25G |
N-(tert-Butoxycarbonyl)-1,4-diaminobutane |
68076-36-8 | >98.0%(GC)(T) | 25g |
￥690.00 | 2024-04-15 | |
| Fluorochem | 210540-1g |
1-Boc-1,4-butanediamine |
68076-36-8 | 98% | 1g |
￡34.00 | 2022-03-01 | |
| Fluorochem | 210540-5g |
1-Boc-1,4-butanediamine |
68076-36-8 | 98% | 5g |
￡63.00 | 2022-03-01 | |
| Fluorochem | 210540-10g |
1-Boc-1,4-butanediamine |
68076-36-8 | 98% | 10g |
￡120.00 | 2022-03-01 |
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NH2-C4-NH-Boc Related Literature
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Aaron R. Funk,Efram Goldberg,Eddie L. Chang,Scott A. Trammell,D. Andrew Knight Dalton Trans. 2013 42 15617
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Karell Pérez-Labrada,Marco A. Cruz-Mendoza,Alejandra Chávez-Riveros,Eduardo Hernández-Vázquez,Tomás Torroba,Luis D. Miranda Org. Biomol. Chem. 2017 15 2450
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Muhammad Nawaz Tahir,Ruben Ragg,Filipe Natalio,Jugal Kishore Sahoo,Phillip Daniel,Kaloian Koynov,Dennis Strand,Susanne Strand,Wolfgang Tremel J. Mater. Chem. B 2015 3 2371
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Filipe Natalio,Anubha Kashyap,Steffen Lorenz,Hannes Kerschbaumer,Michael Dietzsch,Muhammad Nawaz Tahir,Heinz Duschner,Susanne Strand,Dennis Strand,Wolfgang Tremel Nanoscale 2012 4 4680
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Sunxian Yan,Delong Hou,Gaofu Yang,Siyu Pan,Qiuping Xie,Qi Zeng,Zhonghui Wang,Yi Chen,Haojun Fan J. Mater. Chem. A 2019 7 13180
Additional information on NH2-C4-NH-Boc
NH2-C4-NH-Boc: A Comprehensive Overview
The compound with CAS No. 68076-36-8, commonly referred to as NH2-C4-NH-Boc, is a significant molecule in the field of organic chemistry and materials science. Its structure, which includes an amino group (NH2) and a tert-butoxycarbonyl (Boc) protecting group, makes it a versatile building block for various applications. Recent studies have highlighted its potential in drug delivery systems, polymer synthesis, and catalytic processes, underscoring its importance in contemporary research.
NH2-C4-NH-Boc is synthesized through a series of well-established organic reactions, including alkylation and protection/deprotection strategies. The molecule's backbone consists of a four-carbon chain (C4) that connects two amine groups (NH), with one of them being protected by the Boc group. This structure not only enhances stability during synthesis but also facilitates functionalization for specific applications. Researchers have explored its use in creating biocompatible polymers, which are increasingly sought after in biomedical engineering.
One of the most promising areas of research involving NH2-C4-NH-Boc is its application in drug delivery systems. By incorporating this molecule into polymeric matrices, scientists have developed nanocomposites that exhibit controlled drug release profiles. These systems are designed to improve therapeutic efficacy while minimizing side effects, making them highly relevant for personalized medicine approaches. Recent advancements in click chemistry have further expanded the versatility of NH2-C4-NH-Boc, enabling rapid and efficient conjugation with other biomolecules.
In the realm of materials science, NH2-C4-NH-Boc has been utilized as a precursor for synthesizing high-performance polymers. These polymers exhibit exceptional mechanical properties and thermal stability, making them suitable for aerospace and automotive industries. Moreover, the molecule's ability to act as a catalyst in certain reactions has been explored, offering new avenues for sustainable chemical manufacturing processes.
The growing interest in green chemistry has also influenced research on NH2-C4-NH-Boc. Scientists are investigating methods to synthesize this compound using environmentally friendly reagents and conditions. For instance, the use of microwave-assisted synthesis has been reported to significantly reduce reaction times while maintaining product quality. Such innovations align with global efforts to promote sustainable practices in chemical industries.
From an analytical standpoint, the characterization of NH2-C4-NH-Boc has benefited from advanced spectroscopic techniques such as NMR and IR spectroscopy. These methods provide detailed insights into the molecule's structure and dynamic behavior, aiding in the optimization of its synthetic pathways and applications.
In conclusion, NH2-C4-NH-Boc (CAS No. 68076-36-8) stands out as a pivotal compound in modern organic chemistry and materials science. Its unique structure and versatile applications continue to drive innovative research across multiple disciplines. As advancements in synthetic methodologies and material characterization persist, the potential of this compound to contribute to groundbreaking technologies remains immense.
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