B78300
2-Bromopropionic acid
99%
Synonym(s):
(±)-2-Bromopropionic acid
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About This Item
Linear Formula:
CH3CHBrCOOH
CAS Number:
Molecular Weight:
152.97
Beilstein:
1720261
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
99%
form
liquid
refractive index
n20/D 1.475 (lit.)
bp
203 °C (lit.)
density
1.7 g/mL at 25 °C (lit.)
SMILES string
CC(Br)C(O)=O
InChI
1S/C3H5BrO2/c1-2(4)3(5)6/h2H,1H3,(H,5,6)
InChI key
MONMFXREYOKQTI-UHFFFAOYSA-N
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Related Categories
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1A
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
212.0 °F - closed cup
Flash Point(C)
100 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
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Hari M R Gardimalla et al.
Chemical communications (Cambridge, England), (35)(35), 4432-4434 (2005-09-02)
Candida rugosa lipase immobilized on maghemite nanoparticles demonstrated high stereoselectivity in kinetic resolution of racemic carboxylates and improved long-term stability over its parent free enzyme, allowing the supported enzyme to be repeatedly used for a series of chiral resolution reactions.
E A Lock et al.
Archives of toxicology, 74(9), 547-554 (2000-12-29)
Oral administration of L-2-chloropropionic acid (L-CPA) to rats either as a single dose (750 mg/kg) or daily doses (250 mg/kg per day for 3 days) produces selective necrosis to the granule cell layer of the cerebellum. As part of a
O Brandsnes et al.
European journal of biochemistry, 126(2), 247-252 (1982-08-01)
The effect of temperature on the inactivation of liver alcohol dehydrogenase and on the alkylation of a model thiol free in solution by bromoacetate, 2-bromopropionate, 3-bromopropionate and 2-bromo-3-(5-imidazolyl)-propionate has been studied and the thermodynamic activation parameters calculated. All the bromoacids
Jun Zhao et al.
Dental materials : official publication of the Academy of Dental Materials, 27(5), 478-486 (2011-03-08)
The objective of this study was to synthesize and characterize novel hyperbranched poly(acrylic acid)s via atom-transfer radical polymerization (ATRP) technique and tether the photo-curable methacrylate onto the poly(acrylic acid), use these polymers to formulate the resin-modified glass-ionomer cements, and evaluate
Use of structure-activity relationships for probing biochemical mechanisms: glutathione transferase zeta conjugation of haloacids.
P D Swartz et al.
Advances in experimental medicine and biology, 500, 23-31 (2002-01-05)
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