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128013-87-6

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128013-87-6 Usage

General Description

Cis-N-benzyl-4-methylcyclohexan-1-amine is a chemical compound belonging to the class of amines. It is a cyclic compound with a benzyl group attached to the amine nitrogen atom and a methyl group attached to the cyclohexane ring. cis-N-benzyl-4-methylcyclohexan-1-amine has potential applications in organic synthesis and pharmaceutical research, where it can be used as a building block in the production of various compounds. It is important to handle this chemical with caution and to follow proper safety protocols when working with it, due to its potential hazards and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 128013-87-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,0,1 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 128013-87:
(8*1)+(7*2)+(6*8)+(5*0)+(4*1)+(3*3)+(2*8)+(1*7)=106
106 % 10 = 6
So 128013-87-6 is a valid CAS Registry Number.

128013-87-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-4-methylcyclohexan-1-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names I14-5080

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:128013-87-6 SDS

128013-87-6Downstream Products

128013-87-6Relevant articles and documents

Hydride reagents for stereoselective reductive amination. An improved preparation of 3-endo-tropanamine

McGill, John M.,Labell, Elizabeth S.,Williams, MaryAnn

, p. 3977 - 3980 (1996)

The reductive amination of substituted cyclohexanones with sodium triacyloxyborohydrides derived from NaBH4 and various carboxylic acids provides highly diastereoselective conversions to protected axial amines. This method was applied to the stereoselective preparation of 3-endo-tropanamine.

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