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CAS 32345-60-1

Methyl 2-Chloro-L-mandelate TCI M2383

Methyl 2-Chloro-L-mandelate TCI M2383

Chemical Identity

CAS No.
32345-60-1
PubChem
CID 11183258·SID 253661717
Formula
C9H9ClO3
Molecular weight
200.62 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl (2S)-2-(2-chlorophenyl)-2-hydroxyacetate
SMILES
COC(=O)[C@H](C1=CC=CC=C1Cl)O
InChIKey
ZMPGBVQQIQSQED-QMMMGPOBSA-N
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TCI M2383 32345-60-1 Methyl 2-Chloro-L-mandelate is a chiral building block used in asymmetric synthesis to create compounds with specific stereochemical configurations. This compound plays a crucial role in organic chemistry laboratories where precise control over molecular structure is essential. It is particularly valuable in the development of pharmaceuticals and industrial chemicals that require high biological activity and structural specificity. Its chiral nature allows it to participate in enantioselective reactions, making it a key component in the synthesis of optically active compounds.

The compound is known for its stability and solubility in organic solvents, which makes it highly suitable for use in controlled chemical environments. Its molecular structure enables it to serve as a versatile intermediate in various synthetic pathways. The ability to produce specific enantiomers is a major advantage, as it reduces the need for additional purification steps. This characteristic is especially important in the production of drugs where only one enantiomer is therapeutically active.

In Indonesian laboratories, this compound is widely used in organic chemistry research, particularly in the fields of pharmacy and industrial chemistry. Researchers rely on it to develop new compounds with targeted biological activities, such as anti-cancer and antibacterial agents. Its availability and reliability make it a preferred choice for both academic and industrial applications.

TCI brochures (PDF)

  • Asymmetric synthesis is a key application where this compound is used to create enantiomerically pure compounds, essential for pharmaceutical development.
  • Organic chemistry research benefits from its chiral structure, allowing for the synthesis of complex molecules with specific stereochemistry.
  • Pharmaceutical development relies on this compound to produce drugs with high biological activity and selectivity.
  • Industrial chemical synthesis uses it to create compounds with defined stereochemical configurations for specialized applications.
  • Bioactive compound development leverages its properties to design molecules with targeted therapeutic effects in medicinal research.

Brand TCI
CAS number 32345-60-1
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes —
Physical form —
Storage Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry place, away from direct light and moisture to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its chemical integrity. In laboratory settings, it should be handled with care to avoid contamination and ensure safe usage. Due to its chiral nature, it is important to maintain proper labeling and storage conditions to prevent mix-ups with other compounds. Always follow standard laboratory safety protocols when working with this material to ensure both the safety of personnel and the integrity of the compound.

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