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4-Piperidinone, 3-butyl-1-chloro-2,6-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89757-54-0

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89757-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89757-54-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,5 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89757-54:
(7*8)+(6*9)+(5*7)+(4*5)+(3*7)+(2*5)+(1*4)=200
200 % 10 = 0
So 89757-54-0 is a valid CAS Registry Number.

89757-54-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-butyl-1-chloro-2,6-diphenylpiperidin-4-one

1.2 Other means of identification

Product number -
Other names 4-Piperidinone,3-butyl-1-chloro-2,6-diphenyl

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:89757-54-0 SDS

89757-54-0Relevant academic research and scientific papers

Synthesis and PMR Spectral Analysis of Some N-Chloropiperidin-4-ones and N-chloroazabicyclononan-9-ones

Ganapathy, K.,Vijayan, B.

, p. 572 - 574 (2007/10/02)

Various substituted N-chloropiperidin-4-ones and N-chloroazabicyclononan-9-ones have been prepared and they are found to be good oxidising agents.PMR spectra of the substituted N-chloropiperidin-4-ones reveal that they exist in chair conformation.T

Conformational Analysis of Some N-Chloro-2,6-diphenyl-piperidin-4-ones by Kinetic and Equilibrium Methods

Ganapathy, K.,Vijayan, B.

, p. 614 - 616 (2007/10/02)

Confromational analysis of some substituted N-chloro-2,6-diphenylpiperidin-4-ones (I-IX) has been carried out by kinetic and equilibrium methods.The buttressing effect of alkyl substituents on vicinal phenyl groups has been observed during the kinetic and

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