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1H-Pyrazole, 3-(2-chlorophenyl)-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

895138-60-0

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895138-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 895138-60-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,5,1,3 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 895138-60:
(8*8)+(7*9)+(6*5)+(5*1)+(4*3)+(3*8)+(2*6)+(1*0)=210
210 % 10 = 0
So 895138-60-0 is a valid CAS Registry Number.

895138-60-0Downstream Products

895138-60-0Relevant academic research and scientific papers

Facile synthesis of pyrazoles by iron-catalyzed regioselective cyclization of hydrazone and 1,2-diol under ligand-free conditions

Panda, Niranjan,Ojha, Subhadra

, p. 244 - 251 (2018/03/13)

A facile synthesis of pyrazoles by the cyclization of hydrazones and 1,2-diols was described. In the presence of ferric nitrate, the reaction occurs under neat conditions and makes the use of potassium persulfate to oxidize the diol to α-hydroxy carbaldehyde for the reaction with hydrazones to produce 1,3- and 1,3,5-substituted pyrazoles selectively. The overall regioselective transformation occurs in one-pot under ligand-free, mild conditions even in the presence of air.

Fe-catalyzed one-pot synthesis of 1,3-Di- and 1,3,5-trisubstituted pyrazoles from hydrazones and vicinal diols

Panda, Niranjan,Jena, Ashis Kumar

, p. 9401 - 9406,6 (2012/12/11)

An iron-catalyzed route for the regioselective synthesis of 1,3- and 1,3,5-substituted pyrazoles from the reaction of diarylhydrazones and vicinal diols has been developed. This method was found to be practical with wide substrate scope.

Fe-catalyzed one-pot synthesis of 1,3-Di- and 1,3,5-trisubstituted pyrazoles from hydrazones and vicinal diols

Panda, Niranjan,Jena, Ashis Kumar

, p. 9401 - 9406 (2013/01/15)

An iron-catalyzed route for the regioselective synthesis of 1,3- and 1,3,5-substituted pyrazoles from the reaction of diarylhydrazones and vicinal diols has been developed. This method was found to be practical with wide substrate scope.

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