7479-48-3

Basic information

• Product Name: (2E)-2-(2,2-dimethylcyclohexylidene)hydrazinecarboxamide
• CAS NO: 7479-48-3
• Molecular Formula: C₉H₁₇N₃O
• Molecular Weight: 183.2508
• Mol File: 7479-48-3.mol
• Article Data: 1

Chemical Properties

• Density: 1.175g/cm³
• Refractive Index: 1.561
• CAS DataBase Reference: (2E)-2-(2,2-dimethylcyclohexylidene)hydrazinecarboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-2-(2,2-dimethylcyclohexylidene)hydrazinecarboxamide(7479-48-3)
• EPA Substance Registry System: (2E)-2-(2,2-dimethylcyclohexylidene)hydrazinecarboxamide(7479-48-3)

Safety Data

• Hazardous Substances Data: 7479-48-3(Hazardous Substances Data)

Usage

Description

(2E)-2-(2,2-dimethylcyclohexylidene)hydrazinecarboxamide is a hydrazine derivative featuring a cyclohexylidene group. It has the molecular formula C9H18N4O and a molecular weight of 194.27 g/mol. This versatile chemical is known for its potential biological activity, which includes anti-inflammatory, antimicrobial, and anticancer properties.

Uses

Used in Pharmaceutical Research and Drug Development:
(2E)-2-(2,2-dimethylcyclohexylidene)hydrazinecarboxamide is utilized as a pharmaceutical research compound for its potential biological activity. It is particularly valued for its anti-inflammatory, antimicrobial, and anticancer properties, making it a promising candidate for the development of new drugs in these therapeutic areas.
Used as a Building Block in Organic Synthesis:
In addition to its direct applications in drug development, (2E)-2-(2,2-dimethylcyclohexylidene)hydrazinecarboxamide serves as a key building block in the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable component in the creation of complex organic molecules for a wide range of applications across different industries.

Upstream product

• 1193-47-1 2,2-dimethyl-cyclohexanone 
• 854435-09-9 (+/-)-1.1-dimethyl-3-benzoyl-cyclohexanone-⁽²⁾ 
• 563-41-7 semicarbazide hydrochloride 

Downstream Products

• 1193-47-1 2,2-dimethyl-cyclohexanone 

Relevant articles and documents

Reactions of β-trimethylstannylcyclohexanones with peracids: Investigations into the stannyl-directed Baeyer-Villiger reaction

The trimethylstannyl subsituent raises the migratory aptitude of a primary β-carbon to be above that of a not otherwise activated secondary or tertiary carbon. This is apparent from the exclusive formation of the alkene acids 9-11 from Baeyer-Villiger reaction of the β-stannyl cyclohexanones 3-5. The stereoelectronic requirements of the stannyl-directed Baeyer-Villiger reaction were investigated using the axial β-trimethylstannlcyclohexanone 20.