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Sigma-Aldrich

Methyl (R)-(+)-3-bromo-2-methylpropionate

97%

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Synonym(s):
(+)-Methyl (R)-β-bromoisobutyrate
Linear Formula:
BrCH2CH(CH3)CO2CH3
CAS Number:
Molecular Weight:
181.03
Beilstein:
1720833
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

liquid

optical activity

[α]20/D +16°, neat

optical purity

ee: 99% (GLC)

refractive index

n20/D 1.455 (lit.)

bp

85 °C/37 mmHg (lit.)

density

1.422 g/mL at 25 °C (lit.)

SMILES string

COC(=O)[C@@H](C)CBr

InChI

1S/C5H9BrO2/c1-4(3-6)5(7)8-2/h4H,3H2,1-2H3/t4-/m0/s1

InChI key

FKWNAVCXZSQYTA-BYPYZUCNSA-N

Application

Methyl (R)-(+)-3-bromo-2-methylpropionate can be used as a reactant to prepare:
  • (S)-3-(6-Methoxy-pyridin-3-yl)-2-methylpropionic acid methylester by reacting with 5-bromo-2-methoxy pyridine via nucleophilic displacement reaction.
  • Decahydroisoquinoline derivative (NVP-ACQ090) as a potent antagonist of somatostatin sst3 receptor.

It can also be used as a reference compound in the enantioselective alkylation reaction of hydrophobic vitamin B12 derivatives.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

163.4 °F

Flash Point(C)

73 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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The development of a practical synthesis of the potent and selective somatostatin sst3 receptor antagonist [4-(3, 4-difluoro-phenyl)-piperazine-1-yl]-
Banziger M, et al.
Tetrahedron Asymmetry, 14(22), 3469-3477 (2003)
A 1H NMR and molecular modelling investigation of diastereotopic methylene hydrogen atoms.
Tormena CF, et al.
Magnetic Resonance in Chemistry, 40(4), 279-283 (2002)
Hydrophobic vitamin B12. Part 12. Preparation, characterization and enantioselective alkylation of strapped hydrophobic-vitamin B12
Murakami Y, et al.
J. Chem. Soc. Perkin Trans. II, 14(6), 1175-1183 (1995)
Hydrophobic vitamin B12. Part 12. Preparation, characterization and enantioselective alkylation of strapped hydrophobic-vitamin B12.
Murakami Y, et al.
J. Chem. Soc. Perkin Trans. II, 6, 1175-1183 (1995)

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