30134-98-6

Basic information

• Product Name: (cis-4-Aminocyclohexyl)methanol
• Synonyms: cyclohexanemethanol, 4-amino-, cis-
• CAS NO: 30134-98-6
• Molecular Formula: C₇H₁₅NO
• Molecular Weight: 129.2001
• Mol File: 30134-98-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 218.796°C at 760 mmHg
• Flash Point: 86.125°C
• Density: 0.974g/cm³
• Vapor Pressure: 0.026mmHg at 25°C
• Refractive Index: 1.477
• CAS DataBase Reference: (cis-4-Aminocyclohexyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (cis-4-Aminocyclohexyl)methanol(30134-98-6)
• EPA Substance Registry System: (cis-4-Aminocyclohexyl)methanol(30134-98-6)

Safety Data

• Hazardous Substances Data: 30134-98-6(Hazardous Substances Data)

Usage

General Description

(cis-4-Aminocyclohexyl)methanol is a chemical compound with the molecular formula C7H15NO. It is a cyclohexylamine derivative and is commonly used in the production of pharmaceuticals and agrochemicals. (cis-4-Aminocyclohexyl)methanol has a cis configuration, meaning that the substituent groups are on the same side of the carbon-carbon double bond. (cis-4-Aminocyclohexyl)methanol is known for its potential use as a chiral building block in the synthesis of various organic compounds. It also has applications in the production of surfactants, corrosion inhibitors, and other specialty chemicals. Overall, this chemical plays a significant role in the development of various industrial and research applications.

Upstream product

• 60601-18-5 cis 4-benzoylaminocyclohexanemethanol 
• 3306-69-2 2-aza-bicyclo[2.2.2]octan-3-one 
• 61367-16-6 cis-4-aminocyclohexanecarboxylic acid methyl ester hydrochloride 
• 150-13-0 4-amino-benzoic acid 
• 60601-15-2 4-Benzoylamino-cyclohexanecarboxylic acid ethyl ester 

Downstream Products

• 947141-76-6 ((1r,4r)-4-(tert-butoxycarbonylamino)cyclohexyl)methyl 4-methylbenzene-sulfonate 
• 1417615-39-4 C₂₀H₂₆ClN₃O₃ 
• 1272670-06-0 5-(3-(7-oxabtcyclo[2.2.1]heptan-1-ylmethoxy)phenyl)-7-((1S,4S)-4-(aminomethyl)cyclohexyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine 
• 1272667-52-3 5-(3-(7-oxabicyclo[2.2.1]heptan-1-ylmethoxy)phenyl)-7-((1s,4s)-4-(azidomethyl)cyclohexyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine 
• 1272667-53-4 ((1S,4S)-4-(5-(3-(7-oxabicyclo[2.2.1]heptan-1-ylmethoxy)phenyl)-4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)cyclohexyl)methyl methanesulfonate 
• 1272667-38-5 (1S,4S)-4-(5-(3-(7-oxabicyclo[2.2.1]heptan-1-ylmethoxy)phenyl)-4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)cyclohexanecarbaldehyde 
• 1272667-39-6 ((1S,4S)-4-(5-(3-(7-oxabicyclo[2.2.1]heptan-1-ylmethoxy)phenyl)-4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)cyclohexyl)methanol 
• 1272667-35-2 ((1S,4S)-4-(4-amino-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)cyclohexyl)methanol 
• 1272667-36-3 ((1S,4S)-4-(4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)cyclohexyl)methanol 
• 1272667-37-4 ((1S,4S)-4-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)cyclohexyl)methanol 
• 223131-25-7 ((1S,4S)-4-(tert-butoxycarbonylamino)cyclohexyl)methyl 4-methylbenzenesulfonate 

Relevant articles and documents

Approaches towards the synthesis of fluoro(cyclo)alkylamines

The synthesis of fluoro(cyclo)alkylamines 1-amino-6-fluorohexane (1), 1-amino-7-fluoroheptane (2), cis/trans-4-fluorocyclohexylamine (3a,b) and cis-4-fluoromethylcyclohexylamine (4) has been investigated for use as synthons for histamine receptor ligands for use in PET.