CAS 32644-15-8

(2S)-2-Bromopropanoic acid

Description:

(2S)-2-Bromopropanoic acid, with the CAS number 32644-15-8, is an organic compound characterized by its chiral center, which gives it specific stereochemical properties. It features a bromine atom attached to the second carbon of a three-carbon propanoic acid chain, making it a bromo-substituted carboxylic acid. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is soluble in polar solvents like water and alcohols due to the presence of the carboxylic acid functional group, which can engage in hydrogen bonding. The bromine atom contributes to its reactivity, allowing it to participate in various nucleophilic substitution reactions. As a chiral molecule, (2S)-2-Bromopropanoic acid can exhibit different biological activities compared to its enantiomer, making it of interest in pharmaceutical applications. Safety considerations include handling it with care due to its potential irritant properties and the need for proper disposal methods in accordance with chemical safety regulations.

Formula: C₃H₅BrO₂

InChI: InChI=1S/C3H5BrO2/c1-2(4)3(5)6/h2H,1H3,(H,5,6)/t2-/m0/s1

InChI key: InChIKey=MONMFXREYOKQTI-REOHCLBHSA-N

SMILES: [C@H](C(O)=O)(Br)C

Synonyms:

• (-)-2-Bromopropanoic acid
• (-)-2-Bromopropionic acid
• (-)-α-Bromopropanoic acid
• (2S)-2-Bromopropionic acid
• (2S)-2-bromopropanoic acid
• (S)-2-Bromopropanoic acid
• (S)-α-Bromopropionic acid
• <span class="text-smallcaps">L</span>-2-Bromopropionic acid
• <span class="text-smallcaps">L</span>-α-Bromopropionic acid
• Methylbromoacetate
• Propanoic Acid, 2-Bromo-
• Propanoic acid, 2-bromo-, (2S)-
• Propanoic acid, 2-bromo-, (S)-
• Propionic acid, 2-bromo-, (S)-
• L-α-Bromopropionic acid
• (S)-(-)-2-Bromopropionic Acid

(S)-(-)-2-Bromopropionic Acid

CAS: 32644-15-8

Formula: C₃H₅BrO₂

Purity: >98.0%(GC)(T)

Color and Shape: Colorless to Red to Green clear liquid

Molecular weight: 152.98

Ref: 3B-B1757

(2S)-2-bromopropanoic acid

CAS: 32644-15-8

Formula: C₃H₅BrO₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 152.9746

Ref: IN-DA003CDL

(S)-(-)-2-Bromopropionic Acid

CAS: 32644-15-8

(S)-(-)-2-Bromopropionic Acid

Purity: 95%

Color and Shape: Liquid

Molecular weight: 152.97g/mol

Ref: 54-OR71093

(S)-(-)-2-Bromopropionic acid

CAS: 32644-15-8

Purity: 95.0%

Color and Shape: Liquid, Clear

Molecular weight: 152.97500610351562

Ref: 10-F094052

(S)-2-Bromopropionic Acid

Controlled Product

CAS: 32644-15-8

Applications (S)-2-Bromopropionic Acid is an intermediate in the synthesis of structural analogs of the antimitotic tripeptides hemiasterlins as antitumor agents.
References Gamble, W., et al.: Bioorg. Med. Chem., 7, 1611 (1999),

Formula: C₃H₅BrO₂

Color and Shape: Neat

Molecular weight: 152.97

Ref: TR-B686670

(S)-2-Bromopropionic acid

CAS: 32644-15-8

(S)-2-Bromopropionic acid is a synthetic compound that has been shown to bind to an antigen. The structure activity relationship of this compound has been studied in order to find a suitable surrogate for the synthesis of (S)-2-Bromopropionic acid. This compound was synthesized using solid-phase chemistry and the resulting product was purified by HPLC. The synthetic route for (S)-2-Bromopropionic acid included d-alanine, which was used as the biomolecular building block. The alkylation reaction involved the use of chloroacetic acid and methyl iodide, which were reacted with d-alanine in aqueous solution at room temperature. After hydrolysis, ester linkages were introduced with methanol and acetic anhydride. The final product was purified by recrystallization from methanol and acetone.

Formula: C₃H₅BrO₂

Purity: Min. 95%

Color and Shape: Slightly Yellow Clear Liquid

Molecular weight: 152.97 g/mol

Ref: 3D-FB19309