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Pyrano[4,3-c]pyrazol-4(2H)-one, 2-(4-chlorophenyl)-3,6-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106089-52-5

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106089-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106089-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,8 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106089-52:
(8*1)+(7*0)+(6*6)+(5*0)+(4*8)+(3*9)+(2*5)+(1*2)=115
115 % 10 = 5
So 106089-52-5 is a valid CAS Registry Number.

106089-52-5SDS

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 2-(4-chlorophenyl)-3,6-dimethylpyrano[4,3-c]pyrazol-4-one

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:106089-52-5 SDS

106089-52-5Downstream Products

106089-52-5Relevant academic research and scientific papers

SYNTHESIS AND UNAMBIGUOUS ASSIGNMENT OF STRUCTURE TO PYRANOPYRAZOL-4(1H)-ONES AND -4(2H)-ONES

Cantos, Albert,March, Pere De,Moreno-Manas, Marcial,Pla, Anna,Sanchez-Ferrando, Francisco,Virgili, Albert

, p. 295 - 298 (1986)

A clean synthesis of pyranopyrazolones is described.The reactions of 4-chloro-3-(1-chlorovinyl)-6-methyl-2-pyrone with arylhydrazines give pyranopyrazol-4(2H)-ones as the only identified products.However, the isomeric pyranopyrazol-4(1H)-one

Design, synthesis, computational and biological evaluation of some new hydrazino derivatives of DHA and pyranopyrazoles

Kumar, Ajay,Lohan, Poonam,Aneja, Deepak K.,Gupta, Girish Kumar,Kaushik, Dhirender,Prakash, Om

experimental part, p. 81 - 89 (2012/07/14)

Two series of compounds namely, 4-aryl/heteroaryl hydrazino-3-acetyl-6- methyl-2H-pyran-2-ones (4a-4j) and pyrano[4,3-c]pyrazoles (6a-6e and 6g) were synthesized starting from 3-acetyl-4-chloro-6-methyl-2H-pyran-2-one (2). Estimation of pharmacotherapeuti

Synthesis of Pyranopyrazol-4(1H)-ones and -4(2H)-ones from Dehydroacetic Acid. Homo- and Heteronuclear Selective NOE Measurements for Unambiguous Structure Assignment

Cantos, Albert,March, Pedro de,Moreno-Manas, Marcial,Pla, Anna,Sanchez-Ferrando, Francisco,Virgili, Albert

, p. 4425 - 4432 (2007/10/02)

Cyclization of dehydroacetic acid N-substituted hydrazones furnished 1-substituted 3,6-dimethylpyranopyrazol-4(1H)-ones, together with varying amounts of N,N'-disubstituted 5-hydroxy-3-methyl-4-(3-methyl-1H-pyrazol-5-yl)-1H-pyrazoles.The same pyranopyrazolones were obtained regioselectively without side reactions from N-alkylhydrazines and 4-chloro-3-(1-chlorovinyl)-6-methyl-2H-pyran-2-one, ("Dehydroacetchlorid"), while N-arylhydrazines gave the 2-aryl-3,6-dimethylpyranopyrazol-4(2H)-ones.NMR NOE methods, including long-range selective heteronuclear 13C NOE enhancement measurements, allowed unambiguous between -4(1H)-ones and -4(2H)-ones.

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