Diphenylmethyl 7beta-Amino-3-cephem-4-carboxylate TCI D5234

Chemical Identity

Other names: Benzhydryl (6R,7R)-7-Amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate · (6R,7R)-7-Amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid Benzhydryl Ester · 7beta-Amino-3-cephem-4
CAS No.: 36923-21-4
Formula: C20H18N2O3S
Molecular weight: 366.44 g/mol
Purity: >98.0%(HPLC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: benzhydryl (6R,7R)-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
SMILES: C1C=C(N2C(S1)C(C2=O)N)C(=O)OC(C3=CC=CC=C3)C4=CC=CC=C4
InChIKey: NYYBPASOTOAXQW-VQIMIIECSA-N
MDL: MDL23701579
PubChem: CID 9842110

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Diphenylmethyl 7beta-Amino-3-cephem-4-carboxylate is a chemical compound used in asymmetric synthesis to produce bioactive compounds. This material plays a crucial role in laboratory settings where precise control over stereochemistry is required. It is widely utilized in the development of pharmaceuticals and pharmacological agents due to its unique structural features. Its ability to participate in asymmetric reactions makes it a valuable tool for chemists working on complex molecular transformations.

The compound's properties make it a preferred choice for researchers in organic chemistry and pharmacology. Its stable chemical nature allows for easy manipulation under various reaction conditions. The chiral building block nature of this compound enables the synthesis of molecules with high biological activity. Its specificity in chemical reactions ensures that it can be reliably used in a wide range of synthetic pathways.

In Indonesian laboratories, this compound is commonly used by researchers and scientists in the fields of organic chemistry and pharmacology. It is an essential component in the development of new compounds with specific therapeutic effects. Its availability in the local market supports research and development efforts in various academic and industrial institutions. The compound is frequently used in laboratory synthesis applications, contributing to the advancement of drug discovery and chemical innovation.

Asymmetric Synthesis: This compound is ideal for asymmetric synthesis due to its chiral structure, enabling the creation of enantiomerically pure compounds essential for pharmaceutical development.
Pharmaceutical Research: Its use in the synthesis of bioactive compounds makes it a key material for drug discovery and development in pharmaceutical laboratories.
Organic Chemistry Studies: Researchers in organic chemistry benefit from its ability to participate in complex synthetic reactions, supporting the creation of novel molecular structures.
Chiral Compound Development: The compound's role as a chiral building block is crucial in the design of new chiral compounds with specific biological activities.
Bioactive Molecule Synthesis: It is widely used in the synthesis of molecules with high biological activity, contributing to the advancement of medicinal chemistry.

Brand	TCI
CAS number	36923-21-4
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various pack sizes as per supplier specifications
Physical form	Solid (as per standard chemical specifications)
Storage	Store in a cool, dry place away from direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent moisture absorption. Suitable storage containers include glass or high-density polyethylene vessels. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Avoid exposure to heat and direct light to preserve its integrity. Proper ventilation is essential when working with this material in a laboratory setting. Always follow standard safety protocols to ensure safe handling and storage.

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