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4-(Phenylmethylene)-2,4-dihydro-5-(hydroxymethyl)-3H-pyrazol-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87192-03-8

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87192-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87192-03-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,9 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87192-03:
(7*8)+(6*7)+(5*1)+(4*9)+(3*2)+(2*0)+(1*3)=148
148 % 10 = 8
So 87192-03-8 is a valid CAS Registry Number.

87192-03-8Relevant academic research and scientific papers

Arylsulfanyl pyrazolones block mutant SOD1-G93A aggregation. Potential application for the treatment of amyotrophic lateral sclerosis

Chen, Tian,Benmohamed, Radhia,Arvanites, Anthony C.,Ranaivo, Hantamalala Ralay,Morimoto, Richard I.,Ferrante, Robert J.,Watterson, D. Martin,Kirsch, Donald R.,Silverman, Richard B.

experimental part, p. 613 - 622 (2011/03/17)

Amyotrophic lateral sclerosis (ALS) is an orphan neurodegenerative disease currently without a cure. Mutations in copper/zinc superoxide dismutase 1 (SOD1) have been implicated in the pathophysiology of this disease. Using a high-throughput screening assa

TREATMENT OF AMYOTROPHIC LATERAL SCLEROSIS

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Page/Page column 110, (2010/07/10)

The present invention relates to the identification of compounds and pharmaceutical compositions thereof for treating subjects with amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases. The invention also provides methods of preparing the provided compounds.

Ring Construction Using 3-(Arylmethylene)-2,4(3H,5H)-furandione: Synthesis of Pyrazolones and Furobenzothiazepinones

Grob Schmidt, Diane,Zimmer, Hans

, p. 4367 - 4370 (2007/10/02)

The ring transformation of 3-(arylmethylene)-2,4(3H,5H)-furandiones (2) into the corresponding pyrazolones (3) is described.The conversion with selected hydrazines proceeds regioselectively to form a uniquely substituted pyrazolone system (3) as the major

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