Cas 1402732-49-3,1-(2-(3-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)propan-2-one

1402732-49-3

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Basic information

Product Name: 1-(2-(3-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)propan-2-one
Synonyms: 1-(2-(3-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)propan-2-one
CAS NO:1402732-49-3
Molecular Formula:
Molecular Weight: 333.353
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: 1-(2-(3-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)propan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-(3-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)propan-2-one(1402732-49-3)
EPA Substance Registry System: 1-(2-(3-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)propan-2-one(1402732-49-3)

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: 1402732-49-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1402732-49-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,7,3 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1402732-49:
(9*1)+(8*4)+(7*0)+(6*2)+(5*7)+(4*3)+(3*2)+(2*4)+(1*9)=123
123 % 10 = 3
So 1402732-49-3 is a valid CAS Registry Number.

1402732-49-3Upstream product

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1402732-49-3Relevant academic research and scientific papers

Carbon nitride-catalyzed photoredox C-C bond formation with N-aryltetrahydroisoquinolines

Moehlmann, Lennart,Baar, Moritz,Riess, Julian,Antonietti, Markus,Wang, Xinchen,Blechert, Siegfried

supporting information; experimental part, p. 1909 - 1913 (2012/09/25)

In this communication we describe the oxidative C-C bond formation of tertiary amines with various nucleophiles under very mild and environmental friendly conditions by using mesoporous graphitic carbon nitride (mpg-C 3N4) semiconduc

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