(R)-3-Bromo-2-hydroxy-2-methylpropionic Acid TCI B4819

Chemical Identity

CAS No.: 261904-39-6
PubChem: CID 10582468·SID 253660901
Formula: C4H7BrO3
Molecular weight: 183.00 g/mol
Purity: >95.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2R)-3-bromo-2-hydroxy-2-methylpropanoic acid
SMILES: C[C@](CBr)(C(=O)O)O
InChIKey: HBJAYXGUOOININ-BYPYZUCNSA-N

Rp 2.252.250,00

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(R)-3-Bromo-2-hydroxy-2-methylpropionic acid is a chiral building block essential in asymmetric synthesis, playing a critical role in the development of complex molecular structures. This compound is widely used in chemical research to create stereocenters with high enantioselectivity, making it a key component in the synthesis of pharmaceuticals and organic chemicals. Its unique structure, featuring a bromo group, hydroxyl group, and a carboxylic acid group, allows for versatile chemical transformations, including substitution and asymmetric reactions.

The compound's chiral nature and functional group diversity make it a preferred choice for chemists aiming to control stereochemistry in synthetic pathways. Its ability to generate different isomers is crucial in pharmaceutical research, where the biological activity of a compound can vary significantly between enantiomers. This property also enhances its utility in the design of new organic molecules with specific functional properties.

In Indonesian laboratories, this compound is extensively used in both fundamental and applied chemical research. Researchers and academic institutions rely on it to advance their studies in asymmetric synthesis and drug development. Its application spans various fields, including medicinal chemistry and industrial chemical synthesis, where precise control over molecular structure is essential.

TCI brochures (PDF)

Chiral Building Blocks 2025-04-14 · p. 12

Related TCI products

Asymmetric synthesis of pharmaceutical compounds due to its chiral framework and functional group versatility.
Development of new organic molecules with controlled stereochemistry for medicinal and industrial applications.
Research in medicinal chemistry for the synthesis of bioactive compounds with specific enantiomeric purity.
Academic studies in asymmetric catalysis and chiral building block utilization for advanced chemical transformations.
Industrial chemical synthesis requiring precise stereochemical control in the production of specialty chemicals.

Brand	TCI
CAS number	261904-39-6
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per standard chemical supply practices
Physical form	Solid (exact form may vary depending on supplier packaging)
Storage	Store in a cool, dry place away from direct sunlight and moisture

This compound should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could lead to degradation. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment, such as gloves and safety goggles, should be worn. Avoid contact with incompatible substances, and ensure proper disposal in accordance with local regulations. Regular monitoring of storage conditions is advised to ensure the material remains stable and suitable for laboratory use.

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