Cas 1346459-84-4,2-(6-methoxy-3-phenylnaphthalen-2-yl)-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)propanamide

1346459-84-4

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Basic information

Product Name: 2-(6-methoxy-3-phenylnaphthalen-2-yl)-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)propanamide
Synonyms: 2-(6-methoxy-3-phenylnaphthalen-2-yl)-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)propanamide
CAS NO:1346459-84-4
Molecular Formula:
Molecular Weight: 521.434
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-(6-methoxy-3-phenylnaphthalen-2-yl)-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)propanamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(6-methoxy-3-phenylnaphthalen-2-yl)-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)propanamide(1346459-84-4)
EPA Substance Registry System: 2-(6-methoxy-3-phenylnaphthalen-2-yl)-N-(2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl)propanamide(1346459-84-4)

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: 1346459-84-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1346459-84-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,6,4,5 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1346459-84:
(9*1)+(8*3)+(7*4)+(6*6)+(5*4)+(4*5)+(3*9)+(2*8)+(1*4)=184
184 % 10 = 4
So 1346459-84-4 is a valid CAS Registry Number.

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1346459-84-4Relevant academic research and scientific papers

Pd(II)-catalyzed cross-coupling of C(sp2)h bonds and alkyl, aryl, and vinylboron reagents via Pd(II)/Pd(0) catalysis

Wasa, Masayuki,Chan, Kelvin S. L.,Yu, Jin-Quan

, p. 1004 - 1006 (2011/12/05)

Pd(II)-catalyzed cross-coupling of ortho-CH bonds in benzoic acid and phenylacetic acid amides with alkyl, aryl, and vinylboron reagents have been achieved via Pd(II)/Pd(0) catalysis, demonstrating the unprecedented versatility of CH activation reactions.

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