2-Amino-6-oxohexanoic acid

Base Information

• Chemical Name: 2-Amino-6-oxohexanoic acid
• CAS No.: 1962-83-0
• Deprecated CAS: 34897-38-6
• Molecular Formula: C6H11 N O3
• Molecular Weight: 145.158
• DSSTox Substance ID: DTXSID00862802
• Nikkaji Number: J1.136.598A
• Wikipedia: Allysine
• Wikidata: Q61298
• Mol file: 1962-83-0.mol

Synonyms:2-aminoadipate semialdehyde;2-aminoadipic semialdehyde;allysine;alpha-AASA;alpha-aminoadipate semialdehyde

Chemical Property of 2-Amino-6-oxohexanoic acid

Chemical Property:

• Vapor Pressure: 0.000376mmHg at 25°C
• Refractive Index: 1.479
• Boiling Point: 295.2°Cat760mmHg
• Flash Point: 132.3°C
• PSA: 80.39000
• Density: 1.174g/cm³
• LogP: 0.46780
• XLogP3: -3.2
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 145.07389321
• Heavy Atom Count: 10
• Complexity: 124

Purity/Quality:

98%,99%, ^*data from raw suppliers

6-OXO-DL-NORLEUCINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(CC=O)CC(C(=O)O)N
• Uses: A metabolite of Lysine

Technology Process of 2-Amino-6-oxohexanoic acid

There total 2 articles about 2-Amino-6-oxohexanoic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

α-aminoadipate semialdehyde ethyleneacetal (170242-34-9) → α-aminoadipate semialdehyde (1962-83-0)

Guidance literature:

With hydrogenchloride; In water; Heating;

DOI:10.1042/BJ20150009

Reference yield:

→ α-aminoadipate semialdehyde (1962-83-0)

Guidance literature:

α-Amino-ε-hydroxycapronsaeure, CrO3;

Reference yield:

α-aminoadipate semialdehyde (1962-83-0) + 4-amino-benzoic acid (150-13-0,159246-81-8,8014-65-1) → C13H18N2O4

Guidance literature:

With hydrogenchloride; sodium cyanoborohydride; In water; at 37 ℃; for 2h; Darkness;

DOI:10.1021/acs.biochem.7b00409

upstream raw materials:

α-aminoadipate semialdehyde ethyleneacetal