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TCI

CAS 890-98-2

Benzyl DL-Mandelate TCI M0711

Benzyl DL-Mandelate TCI M0711

Chemical Identity

CAS No.
890-98-2
Formula
C15H14O3
Molecular weight
242.27 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
benzyl 2-hydroxy-2-phenylacetate
SMILES
C1=CC=C(C=C1)COC(=O)C(C2=CC=CC=C2)O
InChIKey
JFKWZVQEMSKSBU-UHFFFAOYSA-N
PubChem
CID 13461
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Benzyl DL-Mandelate (TCI M0711, CAS 890-98-2) is a chemical compound widely used in organic synthesis applications. It serves as a key building block in the development of complex molecules, particularly in reactions involving carbonyl reactivity and substitution mechanisms. This compound is valued for its versatility and ability to participate in a variety of chemical transformations, making it essential for researchers working in synthetic chemistry. Its structural complexity allows for diverse chemical interactions, which are crucial in the design of new compounds with specific properties.

The compound’s chemical properties, including its stability under certain conditions, make it a preferred choice in laboratory settings. Its ability to undergo nucleophilic and electrophilic reactions enhances its utility in synthetic pathways. The stability of Benzyl DL-Mandelate ensures that it remains effective during storage and use, reducing the risk of degradation. These characteristics make it a reliable reagent for both academic and industrial research.

In Indonesian laboratories, Benzyl DL-Mandelate is commonly used in organic chemistry research, particularly in higher education institutions and research centers. It is a fundamental component in the synthesis of compounds relevant to pharmaceutical, material science, and food chemistry fields. Its role in creating compounds with specific biological or chemical properties makes it an essential tool for scientific innovation.

  • Organic synthesis applications benefit from Benzyl DL-Mandelate due to its reactivity in carbonyl-based reactions and substitution processes.
  • Pharmaceutical research utilizes this compound in the development of new drugs with targeted biological activities.
  • Material science laboratories use it to create compounds with specific chemical properties for advanced materials.
  • Food chemistry research incorporates it in the synthesis of compounds relevant to flavor and food additives.
  • Academic research institutions rely on Benzyl DL-Mandelate for teaching and experimental purposes in synthetic chemistry.

Brand TCI
CAS number 890-98-2
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes —
Physical form —
Storage Store in a cool, dry place away from light

Benzyl DL-Mandelate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. Proper ventilation is essential when handling this material to minimize inhalation risks. Avoid direct contact with skin and eyes, and use appropriate personal protective equipment. The compound should not be stored near incompatible substances such as strong oxidizers. Regular inspection of storage conditions ensures the integrity of the material remains intact for laboratory use.

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