Cas 94985-11-2,S-<4-(4-fluorophenyl)-5-<4-(methylsulfonyl)phenyl>-1H-pyrrol-2-yl> thiocyanic acid ester

94985-11-2

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Basic information

Product Name: S-<4-(4-fluorophenyl)-5-<4-(methylsulfonyl)phenyl>-1H-pyrrol-2-yl> thiocyanic acid ester
Synonyms: S-<4-(4-fluorophenyl)-5-<4-(methylsulfonyl)phenyl>-1H-pyrrol-2-yl> thiocyanic acid ester
CAS NO:94985-11-2
Molecular Formula:
Molecular Weight: 372.444
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: S-<4-(4-fluorophenyl)-5-<4-(methylsulfonyl)phenyl>-1H-pyrrol-2-yl> thiocyanic acid ester(CAS DataBase Reference)
NIST Chemistry Reference: S-<4-(4-fluorophenyl)-5-<4-(methylsulfonyl)phenyl>-1H-pyrrol-2-yl> thiocyanic acid ester(94985-11-2)
EPA Substance Registry System: S-<4-(4-fluorophenyl)-5-<4-(methylsulfonyl)phenyl>-1H-pyrrol-2-yl> thiocyanic acid ester(94985-11-2)

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: 94985-11-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 94985-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,9,8 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 94985-11:
(7*9)+(6*4)+(5*9)+(4*8)+(3*5)+(2*1)+(1*1)=182
182 % 10 = 2
So 94985-11-2 is a valid CAS Registry Number.

94985-11-2Upstream product

1147550-11-5 ammonium thiocyanate

94985-11-2Downstream Products

94985-10-1 3-(4-fluorophenyl)-2-<4-(methylsulfonyl)phenyl>-5-(methylthio)-1H-pyrrole

94985-11-2Relevant academic research and scientific papers

Antiinflammatory 4,5-Diarylpyrroles: Synthesis and QSAR

Wikerson, Wendell W.,Galbraith, William,Gans-Brangs, Kathleen,Grubb, Mary,Hewes, Walter E.,et al.

, p. 988 - 998 (1994)

A series of 2-substituted- and 2,3-disubstituted-4-(4-fluorophenyl)-5--1H-pyrroles was synthesized and found to be active in the rat adjuvant arthritis model of inflammation.The most active compounds were the 2-halo derivatives i

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