Cas 179749-68-9,N-(5-(bis(2-hydroxyethyl)amino)-2-((4-chloro-5-formylthiazol-2-yl)diazenyl)-4-methoxyphenyl)acetamide

179749-68-9

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Basic information

Product Name: N-(5-(bis(2-hydroxyethyl)amino)-2-((4-chloro-5-formylthiazol-2-yl)diazenyl)-4-methoxyphenyl)acetamide
Synonyms: N-(5-(bis(2-hydroxyethyl)amino)-2-((4-chloro-5-formylthiazol-2-yl)diazenyl)-4-methoxyphenyl)acetamide
CAS NO:179749-68-9
Molecular Formula:
Molecular Weight: 441.895
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-(5-(bis(2-hydroxyethyl)amino)-2-((4-chloro-5-formylthiazol-2-yl)diazenyl)-4-methoxyphenyl)acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(5-(bis(2-hydroxyethyl)amino)-2-((4-chloro-5-formylthiazol-2-yl)diazenyl)-4-methoxyphenyl)acetamide(179749-68-9)
EPA Substance Registry System: N-(5-(bis(2-hydroxyethyl)amino)-2-((4-chloro-5-formylthiazol-2-yl)diazenyl)-4-methoxyphenyl)acetamide(179749-68-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
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Hazardous Substances Data: 179749-68-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 179749-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,7,4 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 179749-68:
(8*1)+(7*7)+(6*9)+(5*7)+(4*4)+(3*9)+(2*6)+(1*8)=209
209 % 10 = 9
So 179749-68-9 is a valid CAS Registry Number.

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179749-68-9Relevant academic research and scientific papers

High nonlinear optical response in 4-chlorothiazole-based azo dyes

Borbone, Fabio,Carella, Antonio,Ricciotti, Laura,Tuzi, Angela,Roviello, Antonio,Barsella, Alberto

experimental part, p. 290 - 295 (2011/06/11)

Four azo dyes showing high nonlinear optical properties were prepared, based on a 4-chlorothiazole azo moiety functionalized with strong acceptor groups and/or further donor/acceptor groups along the conjugated backbone. The effects of the acceptors as we

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