301620
3-Bromo-2-(bromomethyl)propionic acid
97%
Synonym(s):
β,β′-Dibromoisobutyric acid
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Linear Formula:
(BrCH2)2CHCO2H
CAS Number:
Molecular Weight:
245.90
Beilstein:
1752505
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
97%
mp
98-101 °C (lit.)
functional group
bromo
carboxylic acid
SMILES string
OC(=O)C(CBr)CBr
InChI
1S/C4H6Br2O2/c5-1-3(2-6)4(7)8/h3H,1-2H2,(H,7,8)
InChI key
QQZJWQCLWOQDQV-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
3-Bromo-2-(bromomethyl)propionic acid reacts with alkaline arsenite to yield (RS)-3-arsono-2-(hydroxymethyl)propionic acid.[1]
Application
3-Bromo-2-(bromomethyl)propionic acid was used in the synthesis of t-butyl 2-(phenylthiomethyl)propenoate, t-butyl and methyl 3-(phenylthio)-2-(phenylthiomethyl)propenoate and 3-(phenylthio)-2-(phenyl- sulfinylmethyl)propenoate.[2]
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Preparation of t-Butyl 2-(Phenylthiomethyl) propenoate, t-Butyl 3-(Phenylthio)-2-(phenylthiomethyl) propenoate and related compounds.
Haynes RK, et al.
Australian Journal of Chemistry, 37(7), 1571-1578 (1984)
S Chawla et al.
Journal of enzyme inhibition, 8(4), 255-259 (1995-01-01)
(RS)-3-Arsono-2-(hydroxymethyl)propionic acid was synthesized by the action of alkaline arsenite on 3-bromo-2-(bromomethyl)propionic acid. It is a substrate for yeast enolase (EC 4.2.1.11) with a Km of 6.5 mM (for 2-phospho-D-glycerate Km = 0.08 mM). The catalytic constant of the enzyme
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service