Cas 752244-07-8,ethyl 5-formyl-6-phenylimidazo[2,1-b][1,3]thiazole-3-carboxylate

752244-07-8

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Basic information

Product Name: ethyl 5-formyl-6-phenylimidazo[2,1-b][1,3]thiazole-3-carboxylate
Synonyms: ethyl 5-formyl-6-phenyl-imidazo[2,1-b]thiazole-3-carboxylate;ethyl 5-formyl-6-phenylimidazo[2,1-b][1,3]thiazole-3-carboxylate;ethyl 5-methanoyl-6-phenyl-imidazo[2,1-b][1,3]thiazole-3-carboxylate;5-formyl-6-phenyl-3-imidazo[2,1-b]thiazolecarboxylic acid ethyl ester;5-formyl-6-phenyl-imidazo[2,1-b]thiazole-3-carboxylic acid ethyl ester
CAS NO:752244-07-8
Molecular Formula: C15H12N2O3S
Molecular Weight: 300.33
EINECS: N/A
Product Categories: N/A
Mol File: 752244-07-8.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: ethyl 5-formyl-6-phenylimidazo[2,1-b][1,3]thiazole-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 5-formyl-6-phenylimidazo[2,1-b][1,3]thiazole-3-carboxylate(752244-07-8)
EPA Substance Registry System: ethyl 5-formyl-6-phenylimidazo[2,1-b][1,3]thiazole-3-carboxylate(752244-07-8)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: IRRITANT
PackingGroup: N/A
Hazardous Substances Data: 752244-07-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 752244-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,2,2,4 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 752244-07:
(8*7)+(7*5)+(6*2)+(5*2)+(4*4)+(3*4)+(2*0)+(1*7)=148
148 % 10 = 8
So 752244-07-8 is a valid CAS Registry Number.

752244-07-8Upstream product

752244-07-8Downstream Products

752244-07-8Relevant academic research and scientific papers

Synthesis and biological activity of some 3-methyl/ethoxycarbonyl-6-arylimidazo[2,1-b]thiazoles and their 5-bromo/ 5-formyl derivatives

Khazi,Koti,Gadad,Mahajanshetti,Shivakumar,Akki

, p. 393 - 398 (2007/10/03)

Facile reaction of arylacylbromide 1 with 2-amino-4-methylthiazole 2 and its hindered reaction with 2-amino-4-ethoxycarbonylthiazole 3 during the synthesis of 3-methyl/ethoxycarbonyl-6-arylimidazo[2,1-b]thiazoles 8/9 are explained on the basis of electron

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