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4-amino-1-phenyl-cyclohexan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51171-79-0

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51171-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51171-79-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,7 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51171-79:
(7*5)+(6*1)+(5*1)+(4*7)+(3*1)+(2*7)+(1*9)=100
100 % 10 = 0
So 51171-79-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO/c13-11-6-8-12(14,9-7-11)10-4-2-1-3-5-10/h1-5,11,14H,6-9,13H2

51171-79-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Amino-1-phenylcyclohexanol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:51171-79-0 SDS

51171-79-0Downstream Products

51171-79-0Relevant academic research and scientific papers

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

Berglund, Per,Fiorati, Andrea,Humble, Maria S.,Tessaro, Davide

, (2020)

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.).

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