Cas 1246972-40-6,(E)-3-fluoro-5-phenyl-2-(4-(trifluoromethyl)phenyl)-4-(4-(trifluoromethyl)styryl)furan

1246972-40-6

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Basic information

Product Name: (E)-3-fluoro-5-phenyl-2-(4-(trifluoromethyl)phenyl)-4-(4-(trifluoromethyl)styryl)furan
Synonyms: (E)-3-fluoro-5-phenyl-2-(4-(trifluoromethyl)phenyl)-4-(4-(trifluoromethyl)styryl)furan
CAS NO:1246972-40-6
Molecular Formula:
Molecular Weight: 476.393
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: (E)-3-fluoro-5-phenyl-2-(4-(trifluoromethyl)phenyl)-4-(4-(trifluoromethyl)styryl)furan(CAS DataBase Reference)
NIST Chemistry Reference: (E)-3-fluoro-5-phenyl-2-(4-(trifluoromethyl)phenyl)-4-(4-(trifluoromethyl)styryl)furan(1246972-40-6)
EPA Substance Registry System: (E)-3-fluoro-5-phenyl-2-(4-(trifluoromethyl)phenyl)-4-(4-(trifluoromethyl)styryl)furan(1246972-40-6)

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: 1246972-40-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1246972-40-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,9,7 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1246972-40:
(9*1)+(8*2)+(7*4)+(6*6)+(5*9)+(4*7)+(3*2)+(2*4)+(1*0)=176
176 % 10 = 6
So 1246972-40-6 is a valid CAS Registry Number.

1246972-40-6Upstream product

1246972-40-6Downstream Products

1246972-40-6Relevant academic research and scientific papers

Palladium-catalyzed alkenylation of fluoro-substituted furans via C-H activation to form tetrasubstituted furans

Li, Peng,Gu, Ji-Wei,Ying, Yin,He, Yu-Ming,Zhang, Hong-Fei,Zhao, Gang,Zhu, Shi-Zheng

, p. 8387 - 8391 (2010)

A palladium-catalyzed oxidative Heck reaction of fluoro-substituted furans with alkenes was developed to afford tetrasubstituted furans in moderate to good yields.

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