Cas 1396341-90-4,(E)-1-(5-chlorobenzo[d]thiazol-2-yl)-3-(3,4-dimethoxyphenyl)prop-2-en-1-one

1396341-90-4

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Basic information

Product Name: (E)-1-(5-chlorobenzo[d]thiazol-2-yl)-3-(3,4-dimethoxyphenyl)prop-2-en-1-one
Synonyms: (E)-1-(5-chlorobenzo[d]thiazol-2-yl)-3-(3,4-dimethoxyphenyl)prop-2-en-1-one
CAS NO:1396341-90-4
Molecular Formula:
Molecular Weight: 359.833
EINECS: N/A
Product Categories: N/A
Mol File: 1396341-90-4.mol
Article Data: 1

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: (E)-1-(5-chlorobenzo[d]thiazol-2-yl)-3-(3,4-dimethoxyphenyl)prop-2-en-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (E)-1-(5-chlorobenzo[d]thiazol-2-yl)-3-(3,4-dimethoxyphenyl)prop-2-en-1-one(1396341-90-4)
EPA Substance Registry System: (E)-1-(5-chlorobenzo[d]thiazol-2-yl)-3-(3,4-dimethoxyphenyl)prop-2-en-1-one(1396341-90-4)

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: 1396341-90-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1396341-90-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,6,3,4 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1396341-90:
(9*1)+(8*3)+(7*9)+(6*6)+(5*3)+(4*4)+(3*1)+(2*9)+(1*0)=184
184 % 10 = 4
So 1396341-90-4 is a valid CAS Registry Number.

1396341-90-4Upstream product

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1396341-90-4Relevant articles and documents

I2 promoted domino oxidative cyclization for one-pot synthesis of 2-acylbenzothiazoles via metal-free sp3 C-H functionalization

Zhu, Yan-Ping,Lian, Mi,Jia, Feng-Cheng,Liu, Mei-Cai,Yuan, Jing-Jing,Gao, Qing-He,Wu, An-Xin

supporting information, p. 9086 - 9088 (2012/11/07)

An I2 promoted domino protocol was developed to construct 2-acylbenzothiazoles from simple and readily available aromatic ketones/unsaturated methyl ketones and o-aminobenzenethiols. The reaction proceeded smoothly under metal-free and peroxide

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