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19988-39-7

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19988-39-7 Usage

Uses

Used in Chemical Synthesis:
(1R,2S)-2-phenylcyclohexanamine hydrochloride (1:1) is used as a building block in the synthesis of other organic molecules due to its unique stereochemistry and reactivity.
Used in Pharmaceutical Applications:
(1R,2S)-2-phenylcyclohexanamine hydrochloride (1:1) is used as a pharmaceutical agent for its biological activity, potentially offering therapeutic benefits in various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 19988-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,8 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19988-39:
(7*1)+(6*9)+(5*9)+(4*8)+(3*8)+(2*3)+(1*9)=177
177 % 10 = 7
So 19988-39-7 is a valid CAS Registry Number.

19988-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2S)-2-phenylcyclohexan-1-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names Cyclohexanamine,2-phenyl-,hydrochloride,trans

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:19988-39-7 SDS

19988-39-7Downstream Products

19988-39-7Relevant articles and documents

ASYMMETRIC SYNTHESIS OF CIS-2-SUBSTITUTED CYCLOHEXANAMINES WITH HIGHT OPTICAL PURITY

Frahm, A. W.,Knupp, G.

, p. 2633 - 2636 (2007/10/02)

Asymmetric reductive amination of racemic 2-substituted cyclohexanones (R= methyl, ethyl, phenyl, benzyl) using optically active 1-phenyl-ethylamines yields optically active cis-cyclohexanamines.

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