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1H-Pyrazole-4-carboxylic acid, 3-methyl-1-phenyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18093-95-3

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18093-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18093-95-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,9 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18093-95:
(7*1)+(6*8)+(5*0)+(4*9)+(3*3)+(2*9)+(1*5)=123
123 % 10 = 3
So 18093-95-3 is a valid CAS Registry Number.

18093-95-3SDS

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 3-methyl-1-phenyl-1H-pyrazole-4-carboxylic acid methylester

1.2 Other means of identification

Product number -
Other names 3-Methyl-1-phenyl-pyrazolcarbonsaeure-4-methylester

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:18093-95-3 SDS

18093-95-3Downstream Products

18093-95-3Relevant academic research and scientific papers

1,3-Dipolar Cycloadditions, 88. C-Methyl-N-phenylnitrilimine and the Regiochemistry of its Cycloadditions

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

, p. 3039 - 3061 (2007/10/02)

The title compound, a representative of the little known C-alkylnitrilimines, is accessible by three routes: NaNO2 elimination from sodium (α-nitroethylidene)phenylhydrazine in boiling acetonitrile, photolysis of 5-methyl-2-phenyltetrazole, and the thermo

ADDITION DE PHENYLHYDRAZONES AUX OLEFINES EN MILIEU NEUTRE

Fevre, G. Le,Hamelin, J.

, p. 887 - 891 (2007/10/02)

Phenylhydrazones may exhibit three types of reactivity towards alkenes: nucleophilic attack by carbon, nucleophilic attack by nitrogen and 1,3-dipolar cycloaddition through the azomethine imine ylide.The course of the reaction depends on the nature of the hydrazone and alkene substituents.

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