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1H-Pyrazole-4-carboxaldehyde, 5-chloro-3-methyl-1-phenyl-, oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51626-34-7

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51626-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51626-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,2 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51626-34:
(7*5)+(6*1)+(5*6)+(4*2)+(3*6)+(2*3)+(1*4)=107
107 % 10 = 7
So 51626-34-7 is a valid CAS Registry Number.

51626-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde oxime

1.2 Other means of identification

Product number -
Other names 5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-aldoxime

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:51626-34-7 SDS

51626-34-7Relevant academic research and scientific papers

A convenient synthesis, reactions and biological studies of some novel selenolo[2,3-c]pyrazole compounds as antimicrobial and anti-inflammatory agents

Zaki, Remon M.,El-Ossaily, Yasser A.,Geies, Ahmed A.

, p. 893 - 908 (2016/04/20)

5-Chloro-3-methyl-1-phenylpyrazole-4-carbonitrile 3 was reacted with selenium in the presence of sodium borohydride and chloroacetamide to afford selanyl acetamide 5, which underwent Thorpe-Ziegler cyclization upon heating with sodium ethoxide to give the

A convenient synthesis and biological activity of novel thieno[2,3-c]pyrazole compounds as antimicrobial and anti-inflammatory agents

El-Dean, Adel M. Kamal,Zaki, Remon M.,Abdulrazzaq, Abdullah Y.

, p. 97 - 104 (2015/02/05)

A new method for synthesizing 4-amino-3-methyl-1-phenyl-1H-5-substituted thieno[2,3-c]pyrazole was reported. The substituted groups at position 5 include carbonitrile, carboxamide, N-phenyl carboxamide, and benzoyl groups. The newly synthesized compounds

Thieno[2,3-c]pyrazoles and related heterocycles

Haider, Norbert,Farghaly, Abdel-Rahman,Al-Mekhlafi, Nabil,El-Kashef, Hussein

, p. 761 - 765 (2007/10/03)

5-Chloro-3-methyl-1-phenyl-1H-pyrazole-4-carboxaldehyde (1) was converted, via the oxime 2, into the chloronitrile 3. Treatment of compound 3 with methyl thioglycolate gave the novel methyl 4-amino-3-methyl-1-phenyl-1H-thieno [2,3-c]pyrazole-5-carboxylate

GROUP DIPOLE MOMENTS OF SUBSTITUENTS AT POSITIONS 4 AND 5 OF NITROGEN-CONTAINING FIVE-MEMBERED HETEROCYCLES

Fradkina, S. P.,Kvitko, I. Ya.,Alam, L. V.,Fedorova, N. S.

, p. 191 - 196 (2007/10/02)

The dipole moments of the 5-chloro-4-cyano derivatives of oxazole, thiazole, imidazole, and pyrazole were determined.The group dipole moments of substituents at positions 2 and 3 of furan, thiophene, and pyrrole can be used for vector calculation of the dipole moments of various 4- and 5-substituted azoles.

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