Cas 214596-45-9,4-(4-Chloro-phenyl)-4-oxo-3-(1H-thieno[2,3-d]imidazol-2-ylsulfanyl)-butyric acid methyl ester

214596-45-9

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Basic information

Product Name: 4-(4-Chloro-phenyl)-4-oxo-3-(1H-thieno[2,3-d]imidazol-2-ylsulfanyl)-butyric acid methyl ester
Synonyms:
CAS NO:214596-45-9
Molecular Formula:
Molecular Weight: 380.876
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: 4-(4-Chloro-phenyl)-4-oxo-3-(1H-thieno[2,3-d]imidazol-2-ylsulfanyl)-butyric acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-(4-Chloro-phenyl)-4-oxo-3-(1H-thieno[2,3-d]imidazol-2-ylsulfanyl)-butyric acid methyl ester(214596-45-9)
EPA Substance Registry System: 4-(4-Chloro-phenyl)-4-oxo-3-(1H-thieno[2,3-d]imidazol-2-ylsulfanyl)-butyric acid methyl ester(214596-45-9)

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: 214596-45-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 214596-45-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,5,9 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 214596-45:
(8*2)+(7*1)+(6*4)+(5*5)+(4*9)+(3*6)+(2*4)+(1*5)=139
139 % 10 = 9
So 214596-45-9 is a valid CAS Registry Number.

214596-45-9Upstream product

214596-45-9Downstream Products

118879-72-4 [7-(4-Chloro-phenyl)-thieno[3',2':4,5]imidazo[2,1-b]thiazol-6-yl]-acetic acid methyl ester

214596-45-9Relevant academic research and scientific papers

Synthesis of thienoimidazothiazoles

Binder, Dieter,Pyerin, Michael,Schnait, Heinz

, p. 923 - 926 (1998)

Three isomeric substituted thienoimidazothiazoles were synthesized as thiophene analogs of the immune modulator TILOMISOL, by cyclizing appropriate β-oxothioethers of thienoimidazoles. In contrast to the benzene analog no intermediates were observed at this step.

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