2-Amino-4-bromobutanoic acid hydrobromide

Base Information

• Chemical Name: 2-Amino-4-bromobutanoic acid hydrobromide
• CAS No.: 76338-90-4
• Molecular Formula: C4H8 Br N O2 . Br H
• Molecular Weight: 262.929
• Hs Code.: 2922499990
• European Community (EC) Number: 924-737-0
• DSSTox Substance ID: DTXSID30551717
• Mol file: 76338-90-4.mol

Synonyms:2-amino-4-bromobutanoic acid hydrobromide;76338-90-4;2-amino-4-bromobutanoic acid;hydrobromide;2-AMINO-4-BROMOBUTYRIC ACID HYDROBROMIDE;(2S)-2-amino-4-bromobutanoic acid hydrobromide;(+/-)-2-Amino-4-bromobutanoic acid hydrobromide;SCHEMBL1035956;AMY4429;DTXSID30551717;JDLMXICGDYZOJH-UHFFFAOYSA-N;MFCD06809585;AKOS016003592;(S)-2-Amino-4-bromobutyric acid HBr;2-amino-4-bromobutanoicacidhydrobromide;AB89081;4-Bromo-2-aminobutanoic acid hydrobromide;2-Amino-4-bromo-butyric acid hydrobromide;(+/-)-2-AMINO-4-BROMOBUTANOICACIDHBR;alpha-amino-gamma-bromobutyric acid hydrobromide;2-Amino-4-bromobutanoic acid--hydrogen bromide (1/1)

Chemical Property of 2-Amino-4-bromobutanoic acid hydrobromide

Chemical Property:

• PSA: 63.32000
• LogP: 1.84170
• Storage Temp.: Sealed in dry,Room Temperature
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 262.89795
• Heavy Atom Count: 9
• Complexity: 86.1

Purity/Quality:

98% ^*data from raw suppliers

2-Amino-4-bromobutanoic acid hydrobromide 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(CBr)C(C(=O)O)N.Br

Technology Process of 2-Amino-4-bromobutanoic acid hydrobromide

There total 4 articles about 2-Amino-4-bromobutanoic acid hydrobromide 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: 100.0%

α-amino-γ-butyrolactone hydrobromide (6305-38-0) → α-amino-γ-bromobutyric acid hydrobromide (76338-90-4)

Guidance literature:

With hydrogen bromide; acetic acid; at 75 ℃; for 4h;

DOI:10.1139/v03-122

Reference yield:

3-benzoylamino-dihydro-furan-2-one (13602-48-7) → α-amino-γ-bromobutyric acid hydrobromide (76338-90-4)

Guidance literature:

With water; hydrogen bromide;

DOI:10.1021/ja01545a057

Reference yield:

→ α-amino-γ-bromobutyric acid hydrobromide (76338-90-4)

Guidance literature:

With water; hydrogen bromide; at 160 ℃;

upstream raw materials:

3-benzoylamino-dihydro-furan-2-one

α-amino-γ-butyrolactone hydrobromide

Downstream raw materials:

2-aminobutanoic acid

DL-Homoserine

2-amino-4-chloro-butyric acid methyl ester; hydrochloride

2-<(benzyloxycarbonyl)amino>-4-bromobutanoic acid methyl ester