Cas 1415218-79-9,4-fluoro-N-[2-(phenylethynyl)-4-(trifluoromethyl)phenyl]benzamide

1415218-79-9

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Basic information

Product Name: 4-fluoro-N-[2-(phenylethynyl)-4-(trifluoromethyl)phenyl]benzamide
Synonyms: 4-fluoro-N-[2-(phenylethynyl)-4-(trifluoromethyl)phenyl]benzamide
CAS NO:1415218-79-9
Molecular Formula:
Molecular Weight: 383.345
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-fluoro-N-[2-(phenylethynyl)-4-(trifluoromethyl)phenyl]benzamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-fluoro-N-[2-(phenylethynyl)-4-(trifluoromethyl)phenyl]benzamide(1415218-79-9)
EPA Substance Registry System: 4-fluoro-N-[2-(phenylethynyl)-4-(trifluoromethyl)phenyl]benzamide(1415218-79-9)

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: 1415218-79-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1415218-79-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,2,1 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1415218-79:
(9*1)+(8*4)+(7*1)+(6*5)+(5*2)+(4*1)+(3*8)+(2*7)+(1*9)=139
139 % 10 = 9
So 1415218-79-9 is a valid CAS Registry Number.

1415218-79-9Upstream product

536-74-3 phenylacetylene

1415218-79-9Downstream Products

1415218-79-9Relevant academic research and scientific papers

Iodine-catalyzed, stereo- and regioselective synthesis of 4-arylidine-4H-benzo[d][1,3]oxazines and their applications for the synthesis of quinazoline 3-oxides

Lee, Wen-Chun,Shen, Ho-Chuan,Hu, Wan-Ping,Lo, Wei-Sheng,Murali, Chebrolu,Vandavasi, Jaya Kishore,Wang, Jeh-Jeng

, p. 2218 - 2228 (2012)

4-Benzylidene-2-aryl-4H-benzo[d][1,3] oxazines have been synthesized with high stereoselectivity and regioselectivities from 2-alkynylbenzamides in the presence of a catalytic amount of I2. In the reaction mechanism, iodine plays a key role in

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