Cas 1379479-35-2,6-chloro-2-(4,4''-dichloro-[1,1':3',1''-terphenyl]-2'-yl)benzo[d]thiazole

1379479-35-2

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Basic information

Product Name: 6-chloro-2-(4,4''-dichloro-[1,1':3',1''-terphenyl]-2'-yl)benzo[d]thiazole
Synonyms: 6-chloro-2-(4,4''-dichloro-[1,1':3',1''-terphenyl]-2'-yl)benzo[d]thiazole
CAS NO:1379479-35-2
Molecular Formula:
Molecular Weight: 466.818
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: 6-chloro-2-(4,4''-dichloro-[1,1':3',1''-terphenyl]-2'-yl)benzo[d]thiazole(CAS DataBase Reference)
NIST Chemistry Reference: 6-chloro-2-(4,4''-dichloro-[1,1':3',1''-terphenyl]-2'-yl)benzo[d]thiazole(1379479-35-2)
EPA Substance Registry System: 6-chloro-2-(4,4''-dichloro-[1,1':3',1''-terphenyl]-2'-yl)benzo[d]thiazole(1379479-35-2)

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: 1379479-35-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1379479-35-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,4,7 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1379479-35:
(9*1)+(8*3)+(7*7)+(6*9)+(5*4)+(4*7)+(3*9)+(2*3)+(1*5)=222
222 % 10 = 2
So 1379479-35-2 is a valid CAS Registry Number.

1379479-35-2Upstream product

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1379479-35-2Relevant academic research and scientific papers

Pd(II)-catalyzed ortho arylation of 2-arylbenzothiazoles with aryl iodides via benzothiazole-directed C-H activation

Ding, Qiuping,Ji, Huafang,Wang, Dan,Lin, Yuqing,Yu, Weihua,Peng, Yiyuan

supporting information; experimental part, p. 62 - 67 (2012/06/18)

A novel and efficient method for the arylation of 2-arylbenzothiazoles is described via C-H activation. The desired CAr-CAr bond formation proceeded efficiently with good functional-group tolerance and high regioselectivity. Proposed

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