2-(2-Bromo-3-methylbutanamido)acetic acid

Base Information

Chemical Name:2-(2-Bromo-3-methylbutanamido)acetic acid
CAS No.:6940-46-1
Molecular Formula:C7H12BrNO3
Molecular Weight:238.081
Hs Code.:
European Community (EC) Number:230-082-5,654-732-6
NSC Number:163138,60132
DSSTox Substance ID:DTXSID401282370
Wikidata:Q107835711
ChEMBL ID:CHEMBL1966881

Synonyms:2-(2-Bromo-3-methylbutanamido)acetic acid;6940-46-1;NSC163138;2-[(2-bromo-3-methylbutanoyl)amino]acetic acid;52574-83-1;EINECS 230-082-5;(1)-N-(2-Bromo-3-methyl-1-oxobutyl)-glycine;NSC-163138;NSC60132;a-Bromisovalerylglycin;C7H12BrNO3;CHEMBL1966881;SCHEMBL11800572;D,L-BROMOISOVALERYLGLYCINE;DTXSID401282370;NSC 60132;NSC-60132;AKOS024332186;N-(2-Bromo-3-methyl-1-oxobutyl)glycine;NCI60_001229;((2-bromo-3-methylbutanoyl)amino)acetic acid;(+-)-N-(2-bromo-3-methyl-1-oxobutyl)-glycine

Suppliers and Price of 2-(2-Bromo-3-methylbutanamido)acetic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 8 raw suppliers

Chemical Property of 2-(2-Bromo-3-methylbutanamido)acetic acid

Chemical Property:

Vapor Pressure:9.54E-08mmHg at 25°C
Boiling Point:406.5°Cat760mmHg
Flash Point:199.7°C
Density:1.501g/cm³
XLogP3:1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:237.00006
Heavy Atom Count:12
Complexity:182

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C(C(=O)NCC(=O)O)Br

Technology Process of 2-(2-Bromo-3-methylbutanamido)acetic acid

There total 5 articles about 2-(2-Bromo-3-methylbutanamido)acetic 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:

: 56-40-6,18875-39-3,25718-94-9
glycine

: 6940-46-1
N-(α-bromo-isovaleryl)-glycine

Guidance literature:: With sodium hydroxide; -aminoacetic acid;

Reference yield:

: 10323-40-7,565-74-2
2-bromoisovaleric acid

: 6940-46-1
N-(α-bromo-isovaleryl)-glycine

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / 20 - 60 °C / unter allmaehlicher Steigerung der Temperatur

2: NaOH-solution

With sodium hydroxide; thionyl chloride;