306851
2-Bromo-2-methylpropionic acid
98%
Synonym(s):
α-Bromoisobutyric acid, 2-Bromo-2-methylpropionic acid
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About This Item
Linear Formula:
(CH3)2CBrCOOH
CAS Number:
Molecular Weight:
167.00
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-139-2
Beilstein/REAXYS Number:
1745543
MDL number:
Assay:
98%
Quality Level
InChI key
XXSPGBOGLXKMDU-UHFFFAOYSA-N
InChI
1S/C4H7BrO2/c1-4(2,5)3(6)7/h1-2H3,(H,6,7)
SMILES string
CC(C)(Br)C(O)=O
assay
98%
bp
198-200 °C (lit.)
mp
44-47 °C (lit.)
functional group
bromo, carboxylic acid
Related Categories
General description
The multifunctional silica colloids were prepared by coating them with 2-bromo-2-methylpropionic acid stabilized quantum dots.
Application
2-Bromo-2-methylpropionic acid was used in the synthesis of dextran macroinitiator for atom transfer radical polymerization (ATRP) by partial esterification of hydroxyl group of the polysaccharide.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Miseon Yoon et al.
ACS nano, 5(7), 5417-5426 (2011-06-22)
We demonstrate the successful preparation of multifunctional silica colloids by coating with 2-bromo-2-methylpropionic acid (BMPA)-stabilized quantum dots (BMPA-QDs) and BMPA-stabilized iron oxide particles (BMPA-Fe(3)O(4)), along with amine-functionalized poly(amidoamine) (PAMA) dendrimers, using layer-by-layer (LbL) assembly based on a nucleophilic substitution (NS)
Peng Yan et al.
Acta biomaterialia, 10(8), 3786-3794 (2014-05-13)
The fabrication of highly efficient nonviral gene carriers with low cytotoxicity remains a challenge in gene therapy. This paper reports a facile strategy to combine the advantages of gold nanorods (Au NRs) and polycations through surface functionalization. Different Au NR
Raj Kumar Roy et al.
Nature communications, 6, 7237-7237 (2015-05-27)
Biopolymers such as DNA store information in their chains using controlled sequences of monomers. Here we describe a non-natural information-containing macromolecule that can store and retrieve digital information. Monodisperse sequence-encoded poly(alkoxyamine amide)s were synthesized using an iterative strategy employing two
Fabio Salvatore Palumbo et al.
Macromolecular bioscience, 15(11), 1605-1615 (2015-07-03)
Two derivatives of hyaluronic acid (HA) have been synthesized by atom transfer radical polymerization (ATRP), starting from an ethylenediamino HA derivative (HA-EDA) and by using diethylaminoethyl methacrylate (DEAEMA) as a monomer for polymerization. Both samples, indicated as HA-EDA-pDEAEMA a and
Shogo Sasaki et al.
Journal of bioscience and bioengineering, 119(2), 200-205 (2014-07-26)
We demonstrated the synthesis of molecularly imprinted polymers (MIPs) with binding affinity toward a target protein, ribonuclease A (RNase) by atom transfer radical polymerization (ATRP) of acrylic acid, acrylamide, and N,N'-methylenebisacrylamide in the presence of RNase. The binding activity of
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