Cas 1616792-23-4,1-(4-bromophenyl)-2, 2-difluoro-2-(2-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)ethanone

1616792-23-4

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Basic information

Product Name: 1-(4-bromophenyl)-2, 2-difluoro-2-(2-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)ethanone
Synonyms: 1-(4-bromophenyl)-2, 2-difluoro-2-(2-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)ethanone
CAS NO:1616792-23-4
Molecular Formula:
Molecular Weight: 442.303
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-(4-bromophenyl)-2, 2-difluoro-2-(2-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-bromophenyl)-2, 2-difluoro-2-(2-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)ethanone(1616792-23-4)
EPA Substance Registry System: 1-(4-bromophenyl)-2, 2-difluoro-2-(2-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)ethanone(1616792-23-4)

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: 1616792-23-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1616792-23-4 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 1616792-23:
(9*1)+(8*6)+(7*1)+(6*6)+(5*7)+(4*9)+(3*2)+(2*2)+(1*3)=184
184 % 10 = 4
So 1616792-23-4 is a valid CAS Registry Number.

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1616792-23-4Relevant 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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