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147906-04-5

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147906-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147906-04-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,9,0 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 147906-04:
(8*1)+(7*4)+(6*7)+(5*9)+(4*0)+(3*6)+(2*0)+(1*4)=145
145 % 10 = 5
So 147906-04-5 is a valid CAS Registry Number.

147906-04-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Benzyl-4-methylcyclohexanamine hydrochloride (1:1)

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:147906-04-5 SDS

147906-04-5Downstream Products

147906-04-5Relevant articles and documents

Sodium borohydride on wet clay: Solvent-free reductive amination of carbonyl compounds using microwaves

Varma, Rajender S.,Dahiya, Rajender

, p. 6293 - 6298 (2007/10/03)

A solvent-flee reductive amination of carbonyl compounds by wet montmorillonite K 10 clay supported sodium borohydride is described; microwave irradiation facilitates the procedure.

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

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

, p. 3977 - 3980 (2007/10/03)

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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