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ethyl 1,3-diphenyl-4,5-dihydro-1H-pyrazole-5-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87383-50-4

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87383-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87383-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,8 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87383-50:
(7*8)+(6*7)+(5*3)+(4*8)+(3*3)+(2*5)+(1*0)=164
164 % 10 = 4
So 87383-50-4 is a valid CAS Registry Number.

87383-50-4SDS

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 ethyl 2,5-diphenyl-3,4-dihydropyrazole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 2,5-diphenyl-3,4-dihydro-2H-pyrazole-3-carboxylic acid ethyl ester

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:87383-50-4 SDS

87383-50-4Downstream Products

87383-50-4Relevant academic research and scientific papers

Mercuric acetate in organic synthesis: A simple procedure for the synthesis of pyrazolines

Rai, K.M. Lokanatha,Linganna

, p. 3737 - 3744 (2007/10/03)

Reaction of aldehyde hydrazones (1) with mercuric acetate leads to the formation of nitrile imines (2) which can react in situ with olefins to produce 1,3,5-trisubstituted 2-pyrazolines (4) in good yield.

CHLORAMINE-T IN HETEROCYCLIC SYNTHESIS; A SIMPLE PROCEDURE FOR THE GENERATION OF NITRILIMINES AND ITS APPLICATION TO THE SYNTHESIS OF PYRAZOLINES

Rai, Lokanatha,Hassner, Alfred

, p. 2799 - 2808 (2007/10/02)

A new method of generating nitrilimines is described.It involves the reaction of aromatic as well as aliphatic aldehyde hydrazones with chloramine-T.In the presence of olefins pyrazolines are obtained in good yield.

Dihalogentriphenylphosphoranes in Heterocyclic Synthesis; 15. A Simple One-Pot-Procedure for the Generation of Nitrilimines with the Aid of Dihalogentriphenylphosphoranes: 1,3-Dipolar Cycloadditions and 1,5-Electrocyclizations

Wamhoff, Heinrich,Zahran, Magdy

, p. 876 - 879 (2007/10/02)

A simple and versatile one-pot procedure for the in situ generation of nitrilimines from N-acyl hydrazines is described. 1,3-Dipolar cycloadditions and 1,5-electrocyclic ring closures are carried out.Unsymmetrically substituted dipolarophiles show typical

1,3-Dipolar Cycloadditions, 89. New Contributions to the Chemistry of Diphenylnitrilimine

Clovis, James S.,Fliege, Werner,Huisgen, Rolf

, p. 3062 - 3070 (2007/10/02)

Methyl propiolate, tetrolate, and phenylpropiolate combine with diphenylnitrilimine (1) to afford regioisomeric cycloadducts; the preferential orientation shifts in the sequence given from the pyrazole-5-carboxylic ester to the 4-carboxylic ester.Correspo

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