Cas 74675-61-9,2-Furancarboxylic acid, 5-[2-(4-nitrophenyl)-1-[(trichloromethyl)sulfonyl]ethenyl]-, methyl ester, (E)-

74675-61-9

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Basic information

Product Name: 2-Furancarboxylic acid, 5-[2-(4-nitrophenyl)-1-[(trichloromethyl)sulfonyl]ethenyl]-, methyl ester, (E)-
Synonyms:
CAS NO:74675-61-9
Molecular Formula: C15H10Cl3NO7S
Molecular Weight: 454.672
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: 2-Furancarboxylic acid, 5-[2-(4-nitrophenyl)-1-[(trichloromethyl)sulfonyl]ethenyl]-, methyl ester, (E)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Furancarboxylic acid, 5-[2-(4-nitrophenyl)-1-[(trichloromethyl)sulfonyl]ethenyl]-, methyl ester, (E)-(74675-61-9)
EPA Substance Registry System: 2-Furancarboxylic acid, 5-[2-(4-nitrophenyl)-1-[(trichloromethyl)sulfonyl]ethenyl]-, methyl ester, (E)-(74675-61-9)

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: 74675-61-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 74675-61-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,7 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 74675-61:
(7*7)+(6*4)+(5*6)+(4*7)+(3*5)+(2*6)+(1*1)=159
159 % 10 = 9
So 74675-61-9 is a valid CAS Registry Number.

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74675-61-9Relevant academic research and scientific papers

SYNTHESIS OF TRISUBSTITUTED ETHYLENES OF THE FURAN SERIES BASED ON 5-METHOXYCARBONYL-2-FURFURYL TRICHLOROMETHYL SULFONE

Jurasek, Adolf,Kovac, Jaroslav,Belko, Rudolf

, p. 746 - 751 (2007/10/02)

Condensation of 5-methoxycarbonyl-2-furfuryl trichloromethyl sulfone with 4-X-benzaldehydes (X= H, OH, OCH3, N(CH3)2, Cl, I, CN) or 5-Y-2-furaldehydes (Y = H, NO2) in acetic acid in the presence of ammonium acetate and piperidine afforded the correspondin

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