Cas 325829-89-8,[4-(4-chloro-benzenesulfonyl)-4,5-dihydro-1<i>H</i>-pyrazol-3-yl]-(4-chloro-phenyl)-methanone

325829-89-8

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Basic information

Product Name: [4-(4-chloro-benzenesulfonyl)-4,5-dihydro-1H-pyrazol-3-yl]-(4-chloro-phenyl)-methanone
Synonyms: [4-(4-chloro-benzenesulfonyl)-4,5-dihydro-1H-pyrazol-3-yl]-(4-chloro-phenyl)-methanone
CAS NO:325829-89-8
Molecular Formula:
Molecular Weight: 383.255
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: [4-(4-chloro-benzenesulfonyl)-4,5-dihydro-1H-pyrazol-3-yl]-(4-chloro-phenyl)-methanone(CAS DataBase Reference)
NIST Chemistry Reference: [4-(4-chloro-benzenesulfonyl)-4,5-dihydro-1H-pyrazol-3-yl]-(4-chloro-phenyl)-methanone(325829-89-8)
EPA Substance Registry System: [4-(4-chloro-benzenesulfonyl)-4,5-dihydro-1H-pyrazol-3-yl]-(4-chloro-phenyl)-methanone(325829-89-8)

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: 325829-89-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 325829-89-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,5,8,2 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 325829-89:
(8*3)+(7*2)+(6*5)+(5*8)+(4*2)+(3*9)+(2*8)+(1*9)=168
168 % 10 = 8
So 325829-89-8 is a valid CAS Registry Number.

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325829-89-8Relevant academic research and scientific papers

Reactivity of Bifunctional Alkenes with Diazomethane

Reddy, D. Bhaskar,Sarma, M. Rajagopala,Padmaja, A.,Padmavathi, V.

, p. 23 - 32 (2007/10/03)

The cycloaddition of diazomethane to 1-aroyl-2-arylsulfonylethenes (1) and 1,2-bis(arylsulfonyl)ethenes (IV) under different conditions led to a variety of pyrazolines and pyrazoles. The reactivity of pyrazolines was also studied by pyrolysis, nitrosation and acylation.

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