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15443-54-6

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15443-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15443-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,4 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15443-54:
(7*1)+(6*5)+(5*4)+(4*4)+(3*3)+(2*5)+(1*4)=96
96 % 10 = 6
So 15443-54-6 is a valid CAS Registry Number.

15443-54-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dipropylcyclohexanamine

1.2 Other means of identification

Product number -
Other names N,N-di n-propyl cyclohexylamine

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:15443-54-6 SDS

15443-54-6Relevant articles and documents

The direct synthesis of tertiary amines with three different substituents via the reaction of primary amines, alkyl halides, and α-chlorine substituted allylsilanes catalyzed by Lewis acids

Kozuka, Makoto,Tsuchida, Teruko,Mitani, Michiharu

, p. 4527 - 4530 (2005)

Tertiary amines with three different substituents were obtained in a single step by the CuCl/B(OMe)3 or B(OMe)3-catalyzed reaction of α-chlorine substituted allylsilanes, alkyl halides, and primary amines.

Catalytic process

-

, (2008/06/13)

The present invention relates to methods for the reductive amination of a carbonyl-containing compound. R1R2CO where R1and R2are either H, alkyl, aryl or heterocyclic etc with an amine NHR3R4/su

Synthesis of N,N-dialkylcyclohexyl(methylcyclohexyl)amines

Kozlov,Basalaeva

, p. 632 - 636 (2007/10/03)

N,N-Dialkylcyclohexyl(methylcyclohexyl)amines were synthesized by reductive amination of cyclohexanone, cyclohexanol, and their o-, m-, and p-methyl-substituted derivatives with aliphatic nitriles and alcohols, and the steric structure of the products was determined.

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