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TCI

CAS 58632-95-4

2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile TCI B0988

2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile TCI B0988

Chemical Identity

Other names
Boc-ON
CAS No.
58632-95-4
PubChem
CID 5365066·SID 87563941
Formula
C13H14N2O3
Molecular weight
246.26 g/mol
Purity
>98.0%(N)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
tert-butyl [(Z)-[cyano(phenyl)methylidene]amino] carbonate
SMILES
CC(C)(C)OC(=O)O/N=C(\C#N)/C1=CC=CC=C1
InChIKey
QQWYQAQQADNEIC-RVDMUPIBSA-N
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2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile is a chemical compound widely used in organic and biochemical research. It serves as a key reagent in the synthesis of complex molecules, particularly in peptide chemistry and the development of bioactive compounds. This compound is commonly employed in laboratories for its ability to participate in various chemical reactions, including nucleophilic substitution and peptide bond formation. Its structural complexity and functional groups make it a versatile tool for chemists and biochemists.

The compound's high reactivity and stability under controlled conditions make it a preferred choice for laboratory applications. Its molecular structure includes both nitrile and imino groups, which are essential in the synthesis of peptides and other bioactive molecules. These functional groups allow for selective chemical modifications, enabling researchers to design and synthesize complex molecules with specific biological activities. The compound's chemical stability ensures that it remains effective during various experimental procedures.

In Indonesian laboratories, this compound is used in scientific research related to organic chemistry, biochemistry, and pharmacology. Researchers from educational and research institutions utilize it for experiments requiring complex molecular structures and high reactivity. Its role in the synthesis of bioactive compounds makes it a valuable resource for advancing scientific knowledge in these fields.

TCI brochures (PDF)

  • Peptide Synthesis: This compound is ideal for synthesizing peptides due to its nitrile and imino groups, which facilitate peptide bond formation.
  • Bioactive Compound Development: Its reactivity supports the creation of bioactive molecules used in pharmaceutical research and drug development.
  • Organic Chemistry Research: The compound's structural complexity makes it suitable for studying reaction mechanisms and synthetic pathways.
  • Molecular Modification Studies: Its functional groups allow for selective chemical modifications, aiding in the design of new compounds with specific properties.
  • Biomedical Applications: It is used in experiments related to drug discovery and the development of therapeutic agents.

Brand TCI
CAS number 58632-95-4
Molecular formula —
Purity —
Category Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes Available in standard laboratory quantities
Physical form Solid or liquid, depending on the batch
Storage Store in a cool, dry place away from light

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its reactivity, it should be handled in a well-ventilated area, preferably with appropriate personal protective equipment. Avoid contact with incompatible substances such as strong acids or bases. Proper storage ensures the compound remains stable and effective for use in laboratory experiments.

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