Cas 129139-86-2,N-[2-(4-Fluoro-phenyl)-5-methyl-4-nitroso-2H-pyrazol-3-yl]-C-phenyl-methanesulfonamide

129139-86-2

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Basic information

Product Name: N-[2-(4-Fluoro-phenyl)-5-methyl-4-nitroso-2H-pyrazol-3-yl]-C-phenyl-methanesulfonamide
Synonyms: N-[2-(4-Fluoro-phenyl)-5-methyl-4-nitroso-2H-pyrazol-3-yl]-C-phenyl-methanesulfonamide
CAS NO:129139-86-2
Molecular Formula:
Molecular Weight: 374.396
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-[2-(4-Fluoro-phenyl)-5-methyl-4-nitroso-2H-pyrazol-3-yl]-C-phenyl-methanesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[2-(4-Fluoro-phenyl)-5-methyl-4-nitroso-2H-pyrazol-3-yl]-C-phenyl-methanesulfonamide(129139-86-2)
EPA Substance Registry System: N-[2-(4-Fluoro-phenyl)-5-methyl-4-nitroso-2H-pyrazol-3-yl]-C-phenyl-methanesulfonamide(129139-86-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 129139-86-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129139-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,1,3 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 129139-86:
(8*1)+(7*2)+(6*9)+(5*1)+(4*3)+(3*9)+(2*8)+(1*6)=142
142 % 10 = 2
So 129139-86-2 is a valid CAS Registry Number.

129139-86-2Upstream product

129139-86-2Downstream Products

141497-79-2 1-(4-fluorophenyl)-3-methyl-4-amino-5-benzylsulphonamidopyrazole

129139-86-2Relevant academic research and scientific papers

4-Diazo-5-alkylsulphonamidopyrazoles: Synthesis and evaluation of biological activity

Vicentini,Veronese,Giori,Pani,Piras,Gabrielsen,La Colla

, p. 1351 - 1363 (2007/10/02)

A series of 4-diazo-5-alkylsulphonamidopyrazoles (5) was prepared and tested for antitumor, antiviral and antimicrobial activity. Compounds (5a) and (5b) showed a selective, although not very potent cytostatic activity against L1210 and a human T lymphobl

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