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86389-36-8

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86389-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86389-36-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,8 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86389-36:
(7*8)+(6*6)+(5*3)+(4*8)+(3*9)+(2*3)+(1*6)=178
178 % 10 = 8
So 86389-36-8 is a valid CAS Registry Number.

86389-36-8SDS

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 5-(4-methoxyphenyl)-2-methyl-3-phenyl-3,4-dihydropyrazole

1.2 Other means of identification

Product number -
Other names 1H-Pyrazole,4,5-dihydro-3-(4-methoxyphenyl)-1-methyl-5-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:86389-36-8 SDS

86389-36-8Relevant articles and documents

A straightforward synthesis of pyrazolines and pyrazoles: Palladium-catalyzed carbonylative vinylation-cyclocondensation reactions of aryl halides

Wu, Xiao-Feng,Neumann, Helfried,Beller, Matthias

experimental part, p. 4919 - 4924 (2011/10/31)

A novel consecutive one-pot synthesis of pyrazolines and pyrazoles starting from simple aryl halides, styrenes, carbon monoxide, and hydrazines has been established. Palladium-catalyzed carbonylative vinylation of aryl halides gave the corresponding chalcones, which are trapped in situ by addition of hydrazines.

Heterocycles. 3. Synthesis and Spectral Data of Some 2-Pyrazolines

El-Rayyes, Nizar R.,Hovakeemian, George H.,Hmoud, Hayat S.

, p. 225 - 229 (2007/10/02)

The reaction of 1,3-diaryl-2-propen-1-ones (Ia-o) with hydrazine and methyl- and phenylhydrazine produced different substituted 2-pyrazolines (III).The structures of these products were evident from their chemical and spectroscopic analysis.

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