Cas 1609562-79-9,N,N-diethyl-4-chloro-5,6,7,8-tetraphenylisoquinoline-1-carboxamide

1609562-79-9

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Basic information

Product Name: N,N-diethyl-4-chloro-5,6,7,8-tetraphenylisoquinoline-1-carboxamide
Synonyms: N,N-diethyl-4-chloro-5,6,7,8-tetraphenylisoquinoline-1-carboxamide
CAS NO:1609562-79-9
Molecular Formula:
Molecular Weight: 567.13
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: N,N-diethyl-4-chloro-5,6,7,8-tetraphenylisoquinoline-1-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N,N-diethyl-4-chloro-5,6,7,8-tetraphenylisoquinoline-1-carboxamide(1609562-79-9)
EPA Substance Registry System: N,N-diethyl-4-chloro-5,6,7,8-tetraphenylisoquinoline-1-carboxamide(1609562-79-9)

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: 1609562-79-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609562-79-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,5,6 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1609562-79:
(9*1)+(8*6)+(7*0)+(6*9)+(5*5)+(4*6)+(3*2)+(2*7)+(1*9)=189
189 % 10 = 9
So 1609562-79-9 is a valid CAS Registry Number.

1609562-79-9Upstream product

501-65-5 diphenyl acetylene

1609562-79-9Downstream Products

1609562-79-9Relevant academic research and scientific papers

Efficient Synthesis of Isoquinolines via Rh(III)-Catalyzed Oxidative Annulation of Picolinamides with Alkynes

Qian, Zhen-Chao,Zhou, Jun,Li, Bo,Shi, Bing-Feng

, p. 1036 - 1040 (2014)

An efficient synthesis of isoquinolines via Rh(III)-catalyzed oxidative annulation of picolinamides with alkynes using Cu(OAc)2 as an oxidant has been developed. The scope of the reaction was studied with a selection of various picolinamides an

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