Cas 1616792-20-1,2,2-difluoro-2-(2-(2-fluorophenyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)-1-phenylethanone

1616792-20-1

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Basic information

Product Name: 2,2-difluoro-2-(2-(2-fluorophenyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)-1-phenylethanone
Synonyms: 2,2-difluoro-2-(2-(2-fluorophenyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)-1-phenylethanone
CAS NO:1616792-20-1
Molecular Formula:
Molecular Weight: 381.397
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-difluoro-2-(2-(2-fluorophenyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)-1-phenylethanone(CAS DataBase Reference)
NIST Chemistry Reference: 2,2-difluoro-2-(2-(2-fluorophenyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)-1-phenylethanone(1616792-20-1)
EPA Substance Registry System: 2,2-difluoro-2-(2-(2-fluorophenyl)-1,2,3,4-tetrahydroisoquinolin-1-yl)-1-phenylethanone(1616792-20-1)

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: 1616792-20-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1616792-20-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,6,7,9 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1616792-20:
(9*1)+(8*6)+(7*1)+(6*6)+(5*7)+(4*9)+(3*2)+(2*2)+(1*0)=181
181 % 10 = 1
So 1616792-20-1 is a valid CAS Registry Number.

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1616792-20-1Relevant academic research and scientific papers

Visible-light-induced direct C(sp3)-H difluromethylation of tetrahydroisoquinolines with the in situ generated difluoroenolates

Li, Weipeng,Zhu, Xuebin,Mao, Haibin,Tang, Zhongkai,Cheng, Yixiang,Zhu, Chengjian

supporting information, p. 7521 - 7523 (2014/07/07)

An effective approach to C1-difluoromethylated tetrahydroisoquinoline derivatives has been developed through C-H functionalization of tertiary amines by visible-light photoredox catalysis. This method uses stable, easily obtained α,α-difluorinated gem-dio

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