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TCI

CAS 3966-32-3

(R)-(-)-alpha-Methoxyphenylacetic Acid TCI M0830

(R)-(-)-alpha-Methoxyphenylacetic Acid TCI M0830

Chemical Identity

CAS No.
3966-32-3
Formula
C9H10O3
Molecular weight
166.17 g/mol
Purity
>98.0%(GC)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(2R)-2-methoxy-2-phenylacetic acid
SMILES
CO[C@H](C1=CC=CC=C1)C(=O)O
InChIKey
DIWVBIXQCNRCFE-MRVPVSSYSA-N
PubChem
CID 2724294
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(R)-(-)-alpha-Methoxyphenylacetic Acid is a chiral building block widely used in asymmetric synthesis to construct complex molecular structures with specific biological activities. This compound plays a crucial role in organic chemistry laboratories, where it serves as a key component in the development of pharmaceuticals and other bioactive compounds. Its chiral nature allows for precise control over the stereochemistry of synthesized molecules, making it an essential tool for researchers aiming to create enantiomerically pure substances.

The compound’s unique molecular structure, featuring a methoxy group and a carboxylic acid group, contributes to its reactivity and selectivity in asymmetric reactions. These properties make it a preferred choice for chemists working on drug development and synthetic organic chemistry. The compound’s ability to participate in enantioselective transformations enhances its utility in the creation of compounds with specific pharmacological profiles.

In Indonesian laboratories, this material is commonly used by chemists, pharmacologists, and health scientists. It supports the development of new therapeutic agents and industrial applications. Its role in research involving enantiomers and their differing biological activities makes it a valuable resource for advancing scientific understanding and innovation in the field.

  • Asymmetric Synthesis: This compound is ideal for creating chiral molecules with precise stereochemistry, essential for pharmaceutical development.
  • Drug Development: Its use in synthesizing bioactive compounds supports the creation of new therapeutic agents with targeted biological effects.
  • Organic Chemistry Research: It enables the study of complex molecular structures and their interactions in various chemical reactions.
  • Enantiomer Studies: The chiral nature of the compound allows researchers to investigate the differences in biological activity between enantiomers.
  • Pharmaceutical Formulation: It contributes to the synthesis of compounds used in drug manufacturing and formulation processes.

Brand TCI
CAS number 3966-32-3
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid
Storage Store in a cool, dry place away from light 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. Due to its chiral nature, it is important to handle it with care to avoid contamination or unintended stereochemical changes. Proper labeling and storage conditions are essential to ensure the compound remains stable and suitable for use in laboratory applications. Always follow standard safety protocols when handling chemical substances to ensure a safe working environment.

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