1168135-16-7

Basic information

• Product Name: 1-(2-AMino-1-(4-(benzyloxy)phenyl)ethyl)cyclohexanol
• Synonyms: Cyclohexanol, 1-[2-amino-1-[4-(phenylmethoxy)phenyl]ethyl]-
• CAS NO: 1168135-16-7
• Molecular Formula: C₂₁H₂₇NO₂
• Molecular Weight: 325.44458
• Mol File: 1168135-16-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 493.0±30.0 °C(Predicted)
• Appearance: /
• Density: 1.138±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 14.78±0.20(Predicted)
• CAS DataBase Reference: 1-(2-AMino-1-(4-(benzyloxy)phenyl)ethyl)cyclohexanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-AMino-1-(4-(benzyloxy)phenyl)ethyl)cyclohexanol(1168135-16-7)
• EPA Substance Registry System: 1-(2-AMino-1-(4-(benzyloxy)phenyl)ethyl)cyclohexanol(1168135-16-7)

Safety Data

• Hazardous Substances Data: 1168135-16-7(Hazardous Substances Data)

Usage

General Description

The chemical 1-(2-Amino-1-(4-(benzyloxy)phenyl)ethyl)cyclohexanol is a compound with a complex structure, containing an amino group, a cyclohexane ring, and a benzyl ether functional group. It is a secondary amine with a benzyl group attached to the amino group, and a cyclohexanol group attached to the amine group. This chemical may have potential pharmaceutical or medicinal applications due to its structural features, such as its ability to interact with biological receptors or enzymes. Further research and development may be needed to fully understand its properties and potential uses.

Upstream product

• 149289-29-2 N,N-Didesmethyldesvenlafaxine 
• 1076199-24-0 tert-butyl 2-(4-(benzyloxy)phenyl)-2-(1-hydroxycyclohexyl)carbamate 

Downstream Products

• 93413-61-7 1-[2-(dimethylamino)-1-(4-benzyloxyphenyl)ethyl]cyclohexanol 

Relevant articles and documents

1 - [2 - amino - 1 - (4 - benzyloxy-phenyl) ethyl] preparation method of the cyclohexane is mellow and related intermediates

The present invention relates to a preparation method and related intermediates of 1-[2-amino-1-(4-benzyloxyphenyl)-ethyl]-cyclohexanol. The preparation method comprises: taking a compound represented by formula A as raw material, firstly preparing to generate an intermediate compound represented by formula B1 and an intermediate compound represented by formula B2, then taking off a protecting group of the compound represented by the formula B2 to obtain a 1-[2-amino-1-(4-benzyloxyphenyl)-ethyl]-cyclohexanol acid addition salt represented by formula D, and further preparing to obtain 1-[2-amino-1-(4-benzyloxyphenyl)-ethyl]-cyclohexanol. Compared with a conventional method, the raw materials of the method are easy to get and low in price, the product has good quality and high yield, and the method is more suitable for industrialized production.