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

57389-73-8

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57389-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57389-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,8 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57389-73:
(7*5)+(6*7)+(5*3)+(4*8)+(3*9)+(2*7)+(1*3)=168
168 % 10 = 8
So 57389-73-8 is a valid CAS Registry Number.

57389-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-3,4-diphenylpyrazole

1.2 Other means of identification

Product number -
Other names 1-methyl-3,4-diphenyl-1H-pyrazole

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:57389-73-8 SDS

57389-73-8Relevant academic research and scientific papers

C-H bonds as ubiquitous functionality: A general approach to complex arylated pyrazoles via sequential regioselective C-arylation and N-alkylation enabled by SEM-group transposition

Goikhman, Roman,Jacques, Teresa L.,Sames, Dalibor

supporting information; experimental part, p. 3042 - 3048 (2009/09/04)

Pyrazoles are important azole heteroarenes frequently found in pharmaceuticals and protein ligands, and there has been a growing interest in newsynthetic methods for their preparation. We report the first catalytic intermolecular C-H arylation of pyrazole

FORMATION OF PYRAZOLES AND OF IMIDAZOLES FROM PHENACYL KETAL HYDRAZONES OF ALDEHYDES

Scarpetti, David,Kano, Kunio,Anselme, Jean-Pierre

, p. 1073 - 1082 (2007/10/02)

The cyclization of phenacyl ethylene ketal (pek) hydrazones of glyoxals, benzaldehyde and acetaldehyde to pyrazoles is described; in the case of the hydrazones of benzaldehyde and acetaldehyde, the corresponding imidazoles are also formed.A mechanism is suggested for the formation of the imidazoles.

4,5-DIPHENYLIMIDAZOLES FROM THE CYCLIZATION OF BENZIL N-ALKYLMONOHYDRAZONES

Collibee, William L.,Anselme, Jean-Pierre

, p. 655 - 662 (2007/10/02)

The thermal cyclization of monodisubstituted hydrazones (1) affords the corresponding N-substituted-4,5-diphenylimidazoles in good to excellent yields; possible mechanisms for this unusual cyclization are presented.

THE UNUSUAL CYCLIZATION OF BENZIL MONOHYDRAZONES TO 4,5-DIPHENYLIMIDAZOLES

Collibee, William L.,Anselme, Jean-Pierre

, p. 1595 - 1596 (2007/10/02)

Benzil monodisubstituted hydrazones (2) have been shown to undergo cyclodehydration to the corresponding imidazoles (10) and not to pyrazoles as previously reported.

1,3-Dipolar Cycloadditions, 91. The Chemistry of N-Methyl-C-phenylnitrilimine

Fliege, Werner,Grashey, Rudolf,Huisgen, Rolf

, p. 1194 - 1214 (2007/10/02)

The treatment of N'--N-methylhydrazinium bromide, accessible by bromination of benzaldehyde-N-methylhydrazone, with triethylamine furnishes the title compound; this method is superior to the thermolysis and photolysis of 2-methyl-5-phe

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