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27258-04-4

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27258-04-4 Usage

Structure

Symmetric bis-pyrazole compound

Usage

Building block in the synthesis of pharmaceuticals and agrochemicals

Biological Activities

Antifungal, antibacterial, and antitumor properties

Ligand Properties

Bi-dentate ligand, forms coordination complexes with metal ions

Importance

Intermediate in the production of organic compounds

Applications

Medicinal chemistry, materials science

Check Digit Verification of cas no

The CAS Registry Mumber 27258-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,2,5 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27258-04:
(7*2)+(6*7)+(5*2)+(4*5)+(3*8)+(2*0)+(1*4)=114
114 % 10 = 4
So 27258-04-4 is a valid CAS Registry Number.

27258-04-4SDS

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 1,1'-Methylenebis-1H-pyrazole

1.2 Other means of identification

Product number -
Other names -

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:27258-04-4 SDS

27258-04-4Relevant articles and documents

Visalakshi, R.,Jain, V. K.,Kulshreshtha, S. K.,Rao, G. S.

, p. 119 - 124 (1986)

N-Polyazolylmethanes. 1. Synthesis and NMR Study of N,N'-Diazolylmethanes

Julia, Sebastian,Sala, Pilar,Mazo, Jose del,Sancho, Manuel,Ochoa, Carmen,etc.

, p. 1141 - 1145 (2007/10/02)

Thirteen N,N'-diazolylmethanes, including derivatives of pyrazole, imidazole, 1,2,4-triazole, benzimidazole and indazole were prepared by reaction of azoles with methylene chloride under phase transfer catalysis conditions.The relative amounts of isomeric mixtures obtained with 'asymmetric' azoles or with equimolar mixtures of azoles are compared with literature results on monoalkylation of azoles.Proton and carbon-13 nmr spectra of the N,N'-diazolylmethanes are discussed.

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