Cas 1343493-83-3,2,2,2-trifluoro-1-(2-phenyl-4-trifluoromethyl-1,7-phenanthrolin-6-yl)ethane-1,1-diol

1343493-83-3

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Basic information

Product Name: 2,2,2-trifluoro-1-(2-phenyl-4-trifluoromethyl-1,7-phenanthrolin-6-yl)ethane-1,1-diol
Synonyms: 2,2,2-trifluoro-1-(2-phenyl-4-trifluoromethyl-1,7-phenanthrolin-6-yl)ethane-1,1-diol
CAS NO:1343493-83-3
Molecular Formula:
Molecular Weight: 438.329
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: 2,2,2-trifluoro-1-(2-phenyl-4-trifluoromethyl-1,7-phenanthrolin-6-yl)ethane-1,1-diol(CAS DataBase Reference)
NIST Chemistry Reference: 2,2,2-trifluoro-1-(2-phenyl-4-trifluoromethyl-1,7-phenanthrolin-6-yl)ethane-1,1-diol(1343493-83-3)
EPA Substance Registry System: 2,2,2-trifluoro-1-(2-phenyl-4-trifluoromethyl-1,7-phenanthrolin-6-yl)ethane-1,1-diol(1343493-83-3)

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: 1343493-83-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1343493-83-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,3,4,9 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1343493-83:
(9*1)+(8*3)+(7*4)+(6*3)+(5*4)+(4*9)+(3*3)+(2*8)+(1*3)=163
163 % 10 = 3
So 1343493-83-3 is a valid CAS Registry Number.

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1343493-83-3Relevant academic research and scientific papers

Facile and convenient syntheses of fluorine-containing pyrido[2,3- h ]-quinazolines and 1,7-phenanthrolines by condensation reactions of 6,8-bis(trifluoroacetyl)quinolin-5-amine with carbonyl compounds

Hinoshita, Mamoru,Shibata, Dai,Hatakenaka, Mizuki,Okada, Etsuji

, p. 2754 - 2760 (2011)

6,8-Bis(trifluoroacetyl)quinolin-5-amine reacted easily with various aldehydes in the presence of aqueous ammonia to afford trifluoromethylated pyrido[2,3-h]quinazoline derivatives and 1,7-phenanthroline derivatives in good to excellent yields. Under almo

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