Cas no 89711-08-0 (N-Boc-2-aminoacetaldehyde (Technical Grade))

N-Boc-2-aminoacetaldehyde (Technical Grade) is a protected aldehyde derivative widely used in organic synthesis and pharmaceutical intermediates. Its key advantage lies in the Boc (tert-butoxycarbonyl) protecting group, which enhances stability and selectivity during reactions, particularly in peptide coupling and heterocycle formation. The aldehyde functionality allows for further derivatization, making it a versatile building block for amines, imines, and other nitrogen-containing compounds. Technical grade ensures cost-effective suitability for industrial-scale applications where high purity is not critical. The compound’s compatibility with a range of reagents and conditions underscores its utility in multistep synthetic routes. Proper handling under inert conditions is recommended due to its sensitivity to moisture and oxidation.
N-Boc-2-aminoacetaldehyde (Technical Grade) structure
89711-08-0 structure
Product Name:N-Boc-2-aminoacetaldehyde (Technical Grade)
CAS No:89711-08-0
MF:C7H13NO3
MW:159.183022260666
MDL:MFCD01321273
CID:720230
PubChem ID:24870815
Update Time:2025-06-07

N-Boc-2-aminoacetaldehyde (Technical Grade) Chemical and Physical Properties

Names and Identifiers

    • N-Boc-2-aminoacetaldehyde
    • T-Butyl N-(2-Oxoethyl)Cabamate
    • Carbamic acid, N-(2-oxoethyl)-, 1,1-dimethylethyl ester
    • tert-Butyl 2-oxoethylcarbamate
    • tert-butyl N-(2-oxoethyl)carbamate
    • (2-oxo-ethyl)-carbamic acid-tert-butylester
    • (tert-butoxy)-N-(2-oxoethyl)carboxamide
    • 2-(t-butoxycarbonylamino)acetaldehyde
    • boc-l-glycinal
    • N-(tert-butoxycarbonyl)-2-amino-acetaldehyde
    • N-(tert-Butoxycarbonyl)aminoacetaldehyde
    • N-tert-butoxycarbonylglycinal
    • N-tert-butyloxycarbonyl-2-aminoacetaldehyde
    • tert-butyl (2-oxoethyl)carbamate
    • (2-Oxo-ethyl)-carbamic acid tert-butyl ester
    • Carbamic acid, (2-oxoethyl)-, 1,1-dimethylethyl ester
    • boc-glycinal
    • n-boc glycinal
    • zlchem 197
    • N-bocaminoacetaldehyde
    • (bocamino)acetaldehyde
    • N-Boc-aminoacetaldehyde
    • (bocamino) acetaldehyde
    • N-(t-Butoxycarbonyl)glyci
    • Carbamic acid, (2-oxoethyl)-, 1,1-dimethylethyl ester (9CI)
    • (2-Oxoethyl)carbamic acid tert-butyl ester
    • (tert-Butoxycarbonylamino)acetaldehyde
    • 1,1-Dimethylethyl 2-oxoethylcarbamate
    • 2-(tert-Butoxycarbonylamino)ethanal
    • 2-[(tert-Butoxycarbonyl)amino]acetaldehyde
    • Boc-aminoacetaldehyde
    • N-(2-Ketoethyl)carbamic acid tert-butyl ester
    • N-(2-Oxoethyl)carbamic acid tert-butyl ester
    • N-(tert-Butyloxycarbonyl)aminoacetaldehyde
    • N-Boc-glycinal
    • N-tert-Butoxycarbonyl-2-aminoacetaldehyde
    • tert-Butyl (2-oxo-2-(2-(4-(trifluoromethoxy)benzoyl)hydrazinyl)ethyl)carbamate
    • N-Boc-2-aminoacetaldehyde (Technical Grade)
    • tert-butyl formylmethylcarbamate
    • t-butyl N-(2-oxoethyl)carbamate
    • t-butyl (2-oxoethyl)carbamate
    • tert-butyl(2-oxoethyl)carbamate
    • (2-oxo-ethyl)-carbamic tert-butyl ester
    • Boc-glycine Merrifield resin Mesh Size 100-200 Substitution 0.8-1.2 meq/g 1% DVB
    • (2-oxoethyl)-carbamic acid tert-butyl ester
    • 2-(tert-butoxycarbonylamino)acetaldehyde
    • t-butyl (n-2-oxoethyl)carbamate
    • BDBM50137819
    • J-522968
    • DTXSID70401186
    • SCHEMBL248984
    • tert-butyl-N-(2-oxoethyl)carbamate
    • MFCD01321273
    • t-butoxycarbonylarninoacetaldehyde
    • N-Boc-2-aminoacetaldehyde, 95%
    • MFCD00801196
    • N-(t-Butoxycarbonyl)glycinal
    • N-tert-butoxycarbonylaminoacetaldehyde
    • 1,1-dimethylethyl N-(2-oxoethyl)carbamate
    • (2-oxo-ethyl)carbamic acid t-butyl ester
    • N-(2-Oxoethyl)-carbamic acid Tert-Butyl ester
    • t-butyl N-(2-oxoethyl)-carbamate
    • EN300-66991
    • AKOS015950791
    • Boc-Gly-PAM resin (100-200 mesh)
    • t-butyl-n-(2-oxoethyl)carbamate
    • 89711-08-0
    • CHEMBL94805
    • 1,1-dimethylethyl (2-oxoethyl)carbamate
    • MDL： MFCD01321273
    • Inchi： 1S/C7H13NO3/c1-7(2,3)11-6(10)8-4-5-9/h5H,4H2,1-3H3,(H,8,10)
    • InChI Key： ACNRTYKOPZDRCO-UHFFFAOYSA-N
    • SMILES： O=CCNC(OC(C)(C)C)=O

Computed Properties

  • Exact Mass: 159.09000
  • Monoisotopic Mass: 159.08954328g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 4
  • Complexity: 148
  • 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
  • Topological Polar Surface Area: 55.4
  • Surface Charge: 0
  • Tautomer Count: 4
  • XLogP3: 0.5

Experimental Properties

  • Color/Form: Not determined
  • Boiling Point: 237.2°C at 760 mmHg
  • Flash Point: Degrees Fahrenheit:235.4°F
    Degrees Celsius:113°C
  • Refractive Index: n20/D 1.455(lit.)
  • PSA: 55.40000
  • LogP: 1.10090
  • Solubility: Not determined

N-Boc-2-aminoacetaldehyde (Technical Grade) Security Information

N-Boc-2-aminoacetaldehyde (Technical Grade) Pricemore >>

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N-Boc-2-aminoacetaldehyde (Technical Grade) Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Dess-Martin periodinane Solvents: Dichloromethane ;  30 min, rt
1.2 Reagents: Sodium bicarbonate ,  Sodium thiosulfate Solvents: Water ;  30 min, rt
Reference
One-pot synthesis of fused-tetracyclic scaffolds employing a Lewis acid promoted domino reaction of naphthoquinones
Bendiabdellah, Yassine; Villanueva-Margalef, Isabel; Misale, Antonio; Nahar, Kazi S.; Haque, Mohammad R.; et al, Synthesis, 2011, (14), 2321-2333

Production Method 2

Reaction Conditions
1.1 Reagents: Ozone Solvents: Methanol ,  Dichloromethane
1.2 Reagents: Zinc Solvents: Acetic acid
Reference
Synthesis of analogs of 1,3-dihydroxyacetone phosphate and glyceraldehyde 3-phosphate for use in studies of fructose-1,6-diphosphate aldolase
Bischofberger, Norbert; Waldmann, Herbert; Saito, Tohru; Simon, Ethan S.; Lees, Watson; et al, Journal of Organic Chemistry, 1988, 53(15), 3457-65

Production Method 3

Reaction Conditions
1.1 Reagents: Sodium periodate Solvents: Water ;  1 h, rt
Reference
Synthesis of anti-insomnia drug suvorexant
Yuan, Hongshun; Guo, Lei; Pan, Xianhua, Heterocycles, 2021, 102(4), 743-749

Production Method 4

Reaction Conditions
1.1 Reagents: 2-Iodoxybenzoic acid Solvents: Ethyl acetate ;  3 h, reflux
Reference
Stereoselective synthesis of 2-oxyenamides
Krieg, Sara-Cathrin; Grimmer, Jennifer; Pick, Annika Maria; Kelm, Harald; Breugst, Martin; et al, ChemRxiv, 2022, 1, 1-13

Production Method 5

Reaction Conditions
1.1 Reagents: Dess-Martin periodinane Solvents: Dichloromethane ;  2 h, rt
Reference
Total Synthesis of (-)-7-Epicylindrospermopsin, a Toxic Metabolite of the Freshwater Cyanobacterium Aphanizomenon ovalisporum, and Assignment of Its Absolute Configuration
White, James D.; Hansen, Joshua D., Journal of Organic Chemistry, 2005, 70(6), 1963-1977

Production Method 6

Reaction Conditions
1.1 Reagents: Sodium periodate Solvents: Water ;  2 h, rt
Reference
Synthesis of a peptide nucleic acid with a novel 1-methyl-6-mercaptopurine base
Aboul-Fadl, Tarek; Rajeev, Gopalan; Broom, Arthur D., Journal of Heterocyclic Chemistry, 2008, 45(2), 445-451

Production Method 7

Reaction Conditions
1.1 Reagents: Lithium aluminum hydride Solvents: Tetrahydrofuran ;  10 min, 0 °C
1.2 Reagents: Water
Reference
A C-terminal aldehyde insect kinin analog enhances inhibition of weight gain and induces significant mortality in Helicoverpa zea larvae
Nachman, Ronald J.; Coast, Geoffrey M.; Douat, Celine; Fehrentz, Jean-Alain; Kaczmarek, Krzyztoff; et al, Peptides (New York, 2003, 24(10), 1615-1621

Production Method 8

Reaction Conditions
1.1 Reagents: Sodium periodate Solvents: Water ;  1 h, rt
Reference
A Small Molecule That Switches a Ubiquitin Ligase From a Processive to a Distributive Enzymatic Mechanism
Kathman, Stefan G.; Span, Ingrid; Smith, Aaron T.; Xu, Ziyang; Zhan, Jennifer; et al, Journal of the American Chemical Society, 2015, 137(39), 12442-12445

Production Method 9

Reaction Conditions
1.1 Reagents: Sodium periodate Solvents: Water ;  1 h, rt
Reference
Identification of non-peptidic cysteine reactive fragments as inhibitors of cysteine protease rhodesain
McShan, Danielle; Kathman, Stefan; Lowe, Brittiney; Xu, Ziyang; Zhan, Jennifer; et al, Bioorganic & Medicinal Chemistry Letters, 2015, 25(20), 4509-4512

Production Method 10

Reaction Conditions
1.1 Reagents: Sodium periodate Solvents: Water ;  1 h, 23 °C
Reference
A Fragment-Based Method to Discover Irreversible Covalent Inhibitors of Cysteine Proteases
Kathman, Stefan G.; Xu, Ziyang; Statsyuk, Alexander V., Journal of Medicinal Chemistry, 2014, 57(11), 4969-4974

N-Boc-2-aminoacetaldehyde (Technical Grade) Raw materials

N-Boc-2-aminoacetaldehyde (Technical Grade) Preparation Products

N-Boc-2-aminoacetaldehyde (Technical Grade) Related Literature

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