Cas 6692-20-2,Ethanone, 2-(2-imino-3-thiazolidinyl)-1-(4-methoxyphenyl)-, monohydrobromide

6692-20-2

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Basic information

Product Name: Ethanone, 2-(2-imino-3-thiazolidinyl)-1-(4-methoxyphenyl)-, monohydrobromide
Synonyms:
CAS NO:6692-20-2
Molecular Formula: C12H14N2O2S.BrH
Molecular Weight: 331.233
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: Ethanone, 2-(2-imino-3-thiazolidinyl)-1-(4-methoxyphenyl)-, monohydrobromide(CAS DataBase Reference)
NIST Chemistry Reference: Ethanone, 2-(2-imino-3-thiazolidinyl)-1-(4-methoxyphenyl)-, monohydrobromide(6692-20-2)
EPA Substance Registry System: Ethanone, 2-(2-imino-3-thiazolidinyl)-1-(4-methoxyphenyl)-, monohydrobromide(6692-20-2)

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: 6692-20-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 6692-20-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,9 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6692-20:
(6*6)+(5*6)+(4*9)+(3*2)+(2*2)+(1*0)=112
112 % 10 = 2
So 6692-20-2 is a valid CAS Registry Number.

6692-20-2Upstream product

6692-20-2Downstream Products

92754-18-2 6-(4-Methoxy-phenyl)-2,3-dihydro-imidazo[2,1-b]thiazole

6692-20-2Relevant academic research and scientific papers

Substituted 6-phenylimidazo[2,1-b]]thiazoles and thiazolines as potential cardiotonic agents

Andreani,Rambaldi,Bonazzi,et al.

, p. 219 - 222 (2007/10/02)

A series of phenylimidazo[2,1-b]thiazoles and thiazolines bearing one or two methoxy groups in different positions of the phenyl ring was synthesized and tested on isolated guinea pig atria. Two compounds showed a strong positive inotropic activity.

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