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Butanamide, 2,2-dimethyl-3-[(4-nitrophenyl)hydrazono]-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

140887-68-9

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140887-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140887-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,8,8 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 140887-68:
(8*1)+(7*4)+(6*0)+(5*8)+(4*8)+(3*7)+(2*6)+(1*8)=149
149 % 10 = 9
So 140887-68-9 is a valid CAS Registry Number.

140887-68-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethyl-3-[(4-nitrophenyl)hydrazinylidene]-N-phenylbutanamide

1.2 Other means of identification

Product number -
Other names Butanamide,2,2-dimethyl-3-[(4-nitrophenyl)hydrazono]-N-phenyl

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:140887-68-9 SDS

140887-68-9Relevant academic research and scientific papers

Inter-and intra-molecular cyclisation reactions of azoacetates derived from aryl hydrazones of ethyl acetoacetate and acetoacetanilides

O'Halloran, Neil,James, John P.,Downey, Carol A.,O'Malley, Patrick,Duff, Thomas,Bertrand, Samuel

experimental part, p. 2681 - 2701 (2011/04/16)

The base induced cyclisations of azoacetates to azetidinones were investigated. In addition to the isolation of the desired products, it was found that 2-iminopyrrolidine-5-one derivatives as well as N-acyl hydrazides could be isolated when metal cyanides were employed as base. These entities were further modified to form pyrrolidine-2,5-diones and diazetidinones respectively. The Japan Institute of Heterocyclic Chemistry.

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