Cas 4335-32-4,6-(4-CHLOROPHENYL)-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE

4335-32-4

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Basic information

Product Name: 6-(4-CHLOROPHENYL)-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE
Synonyms: 6-(4-CHLOROPHENYL)-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE;BUTTPARK 4\01-73
CAS NO:4335-32-4
Molecular Formula: C₁₁H₉ClN₂S
Molecular Weight: 236.72
EINECS: N/A
Product Categories: N/A
Mol File: 4335-32-4.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 445.5°C at 760 mmHg
Flash Point: 223.2°C
Appearance: /
Density: 1.44g/cm³
Vapor Pressure: 3.94E-08mmHg at 25°C
Refractive Index: 1.726
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 6-(4-CHLOROPHENYL)-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE(CAS DataBase Reference)
NIST Chemistry Reference: 6-(4-CHLOROPHENYL)-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE(4335-32-4)
EPA Substance Registry System: 6-(4-CHLOROPHENYL)-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE(4335-32-4)

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: 4335-32-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 4335-32-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,3 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4335-32:
(6*4)+(5*3)+(4*3)+(3*5)+(2*3)+(1*2)=74
74 % 10 = 4
So 4335-32-4 is a valid CAS Registry Number.

InChI:InChI=1/C11H9ClN2S/c12-9-3-1-8(2-4-9)10-7-14-5-6-15-11(14)13-10/h1-4,7H,5-6H2

4335-32-4Upstream product

4335-32-4Downstream Products

4335-32-4Relevant academic research and scientific papers

Synthetic and Mechanistic Studies on the Preparation of Pyridyl-Substituted Imidazothiazoles

Lantos, Ivan,Gombatz, Kerry,McGuire, Michael,Pridgen, Lendon,Remich, James,Shilcrat, Susan

, p. 4223 - 4227 (2007/10/02)

A new method is presented for the introduction of the 4'-pyridyl substituent into 6-aryl-2,3-dihydroimidazothiazoles.The method involves treatment of the imidazothiazolines with the reactive complex of pyridine and ethyl chloroformate and oxidative deethyl carboxylation of the dihydropyridine adducts formed.Sulfur in refluxing mesitylene was found most suitable for the latter reaction, but chromium trioxide in pyridine or KtBuO and air were also effective.

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