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ChemicalBook--->CAS DataBase List--->110556-33-7

110556-33-7

110556-33-7 Structure

110556-33-7 Structure
IdentificationBack Directory
[Name]

METHYL (R)-(+)-3-BROMO-2-METHYLPROPIONATE
[CAS]

110556-33-7
[Synonyms]

METHYL (R)-(+)-3-BROMOISOBUTYRATE
(+)-methyl (r)-β-bromoisobutyrate
methyl 3-bromo-2-methylpropionate
(+)-METHYL (R)-BETA-BROMOISOBUTYRATE
(R)-Methyl 3-bromo-2-methylpropanoate
Methyl (R)-(+)-3-Bromoisobutyrate >
methyl (2R)-3-bromo-2-methylpropanoate
Methyl (R)-(+)-3-Bromoisobutyrate
(+)-METHYL (R)-3-BROMO-2-METHYLPROPIONATE
METHYL (R)-(+)-3-BROMO-2-METHYLPROPIONATE
(+)-methyl (R)-3-bromo-2-methyl propionate
(R)-(+)-3-BROMOISOBUTYRIC ACID METHYL ESTER
Methyl (R)-(+)-3-bromo-2-methylpropionate 97%
(R)-2-Methyl-3-bromopropionic acid methyl ester
(R)-3-Bromo-2-methylpropanoic acid methyl ester
(R)-(+)-3-BROMO-2-METHYLPROPIONIC ACID METHYL ESTER
Propanoic acid, 3-bromo-2-methyl-, methyl ester, (2R)-
METHYL (R)-(+)-3-BROMO-2-METHYLPROPIONAT E, 97% (99% EE/GLC)
(R)-(+)-3-Bromoisobutyric Acid Methyl Ester (R)-(+)-3-Bromo-2-Methylpropionic Acid Methyl Ester Methyl (R)-(+)-3-Bromo-2-methylpropionate
[Molecular Formula]

C5H9BrO2
[MDL Number]

MFCD00010639
[MOL File]

110556-33-7.mol
[Molecular Weight]

181.03
Chemical PropertiesBack Directory
[Boiling point ]

85 °C37 mm Hg(lit.)
[density ]

1.422 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.455
[Fp ]

165 °F
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

liquid
[optical activity]

[α]20/D +16°, neat
[BRN ]

1720833
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[HS Code ]

2915907098
Hazard InformationBack Directory
[Uses]

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.
Spectrum DetailBack Directory
[Spectrum Detail]

METHYL (R)-(+)-3-BROMO-2-METHYLPROPIONATE(110556-33-7)1HNMR
METHYL (R)-(+)-3-BROMO-2-METHYLPROPIONATE(110556-33-7)FT-IR
METHYL (R)-(+)-3-BROMO-2-METHYLPROPIONATE(110556-33-7)IR
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