177906-46-6

Basic information

• Product Name: Cyclohexanol, 4-amino-1-methyl-, cis- (9CI)
• Synonyms: Cyclohexanol, 4-amino-1-methyl-, cis- (9CI);cis-4-Amino-1-methylcyclohexanol;cis-4-AMino-1-Methylcyclo...;(1s,4s)-4-aMino-1-Methylcyclohexanol;cis-4-Amino-1-methylcyclohexan-1-ol;cis-4-Hydroxy-4-methylcyclohexan-1-amine, cis-4-Amino-1-hydroxy-1-methylcyclohexane;Cyclohexanol,4-amino-1-methyl-,cis-
• CAS NO: 177906-46-6
• Molecular Formula: C₇H₁₅NO
• Molecular Weight: 129.2001
• Product Categories: AMINEPRIMARY
• Mol File: 177906-46-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 203℃
• Flash Point: 77℃
• Appearance: /
• Density: 0.998
• Storage Temp.: 2-8°C(protect from light)
• PKA: 15.19±0.40(Predicted)
• CAS DataBase Reference: Cyclohexanol, 4-amino-1-methyl-, cis- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanol, 4-amino-1-methyl-, cis- (9CI)(177906-46-6)
• EPA Substance Registry System: Cyclohexanol, 4-amino-1-methyl-, cis- (9CI)(177906-46-6)

Safety Data

• Hazardous Substances Data: 177906-46-6(Hazardous Substances Data)

Usage

General Description

Cyclohexanol, 4-amino-1-methyl-, cis- (9CI) is a chemical compound with the molecular formula C7H15NO. It is an aminocyclohexanol compound with a methyl group and an amino group attached to the cyclohexane ring in the cis configuration. This chemical is commonly used in organic synthesis and pharmaceutical research as a building block for the synthesis of various molecules. It may also have potential applications in the development of new drugs and pharmaceuticals due to its unique chemical structure and properties. Additionally, it is important to handle and store this compound carefully as it may pose health and safety risks if mishandled.

Upstream product

• 17429-02-6 4-hydroxy-4-methylcyclohexanone 
• 4746-97-8 cyclohexanedione monoethylene ketal 
• 66336-42-3 8-methyl-1,4-dioxa-spiro[4.5]decan-8-ol 

Downstream Products

• 59477-37-1 4-methylcyclohex-3-enamine 
• 291756-09-7 tert-butyl (4-methylcyclohex-3-en-1-yl)carbamate 
• 1403864-55-0 tert-butyl 3-hydroxy-4-methylcyclohexylcarbamate 
• 25577-22-4 N-(4-methyl-cyclohex-3-enyl)-phthalimide 

Relevant articles and documents

Application of Transaminases in a Disperse System for the Bioamination of Hydrophobic Substrates

The challenging bioamination of hydrophobic substrates has been attained through the employment of a disperse system consisting of a combination of a low polarity solvent (e. g. isooctane or methyl-tert-butylether), a non-ionic surfactant and a minimal amount of water. In these conditions, amine transaminases (ATA) were shown to efficiently carry out the reductive amination of variously substituted cyclohexanones, providing good conversions often coupled with a superior stereoselectivity if compared with the corresponding chemical reductive amination. An array of synthetically useful 4-substituted aminocyclohexanes was consequentially synthesized through biocatalysis, analyzed and stereochemically characterized. (Figure presented.).

N-(4-HYDROXY-4-METHYL-CYCLOHEXYL)-4-PHENYL-BENZENESULFONAMIDES AND N-(4-HYDROXY-4-METHYL-CYCLOHEXYL)-4-(2-PYRIDYL)BENZENESULFONAMIDES AND THEIR THERAPEUTIC USE

The present invention pertains generally to the field of therapeutic compounds. More specifically the present invention pertains to certain substituted N-(4-hydroxy-4- methyl-cyclohexyl)-4-phenyl-benzenesulfonamide and N-(4-hydroxy-4-methyl- cyclohexyl)-4