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694-48-4

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694-48-4 Usage

Uses

1,3-Dimethylpyrazole (cas# 694-48-4) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 694-48-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 694-48:
(5*6)+(4*9)+(3*4)+(2*4)+(1*8)=94
94 % 10 = 4
So 694-48-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H8N2/c1-5-3-4-7(2)6-5/h3-4H,1-2H3

694-48-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Dimethylpyrazole

1.2 Other means of identification

Product number -
Other names 1H-Pyrazole, 1,3-dimethyl-

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:694-48-4 SDS

694-48-4Relevant articles and documents

Chromatographic component of identification of the transformation products of 1,1-dimethylhydrazine in the presence of sulfur

Zenkevich,Ul'Yanov,Golub,Buryak

, p. 1106 - 1114 (2014/08/05)

The gas-chromatographic retention indices of the products of 1,1-dimethylhydrazine transformations in the presence of sulfur allows one to confirm and, in ceratin cases, make more exact the results of their gas chromatography-mass spectrometry identificat

New synthesis and properties of 3-alkyl-, 3-chloroalkyl-, 3-perfluoroalkyl-, and 3-aryl-1-methyl-(5-halo)pyrazoles from chloro(bromo) vinyl ketones and N,N-dimethylhydrazine

Levkovskaya,Bozhenkov,Larina,Mirskova

, p. 1501 - 1506 (2007/10/03)

A new regioselective heterocyclization was revealed in the reaction of 2-chloro- and 2,2-dichloro-(bromo)vinyl ketones with N,N-dimethylhydrazine to afford 3-substituted 1-methyl(5-halo)pyrazoles. The reaction is accompanied by elimination of methyl halide and formation of up to 90% of N,N,N-trimethylhydrazinium halide as the second product.

Systemic fungicides. The synthesis of certain pyrazole analogues of carboxin

Huppatz

, p. 135 - 147 (2007/10/02)

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