Cas 216663-43-3,3-(1,1-Dimethylethyl) 5-benzyl 2-(((trifluoromethyl)carbonyl)amino)-4-methylthiophene-3,5-dicarboxylate

216663-43-3

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Basic information

Product Name: 3-(1,1-Dimethylethyl) 5-benzyl 2-(((trifluoromethyl)carbonyl)amino)-4-methylthiophene-3,5-dicarboxylate
Synonyms: 3-(1,1-Dimethylethyl) 5-benzyl 2-(((trifluoromethyl)carbonyl)amino)-4-methylthiophene-3,5-dicarboxylate
CAS NO:216663-43-3
Molecular Formula:
Molecular Weight: 443.444
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: 3-(1,1-Dimethylethyl) 5-benzyl 2-(((trifluoromethyl)carbonyl)amino)-4-methylthiophene-3,5-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: 3-(1,1-Dimethylethyl) 5-benzyl 2-(((trifluoromethyl)carbonyl)amino)-4-methylthiophene-3,5-dicarboxylate(216663-43-3)
EPA Substance Registry System: 3-(1,1-Dimethylethyl) 5-benzyl 2-(((trifluoromethyl)carbonyl)amino)-4-methylthiophene-3,5-dicarboxylate(216663-43-3)

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: 216663-43-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 216663-43-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,6,6 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 216663-43:
(8*2)+(7*1)+(6*6)+(5*6)+(4*6)+(3*3)+(2*4)+(1*3)=133
133 % 10 = 3
So 216663-43-3 is a valid CAS Registry Number.

216663-43-3Upstream product

216663-40-0 2-benzyl 4-(tert-butyl) 5-amino-3-methyl-thiophene-2,4-dicarboxylate

216663-43-3Downstream Products

216663-43-3Relevant academic research and scientific papers

Synthesis and use of thiophene- and pyrrole-based heteroaromatic compounds

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, (2008/06/13)

Methods for preparing thiophene and pyrrole-based heterocyclic compounds are disclosed. Also disclosed are libraries of thiophene and pyrrole-based heterocyclic compounds, methods for preparing the libraries of thiophene and pyrrole-based heterocyclic compounds, and methods for using the thiophene and pyrrole-based heterocyclic compounds and compound libraries of the invention. The compounds of the invention have biological activity including anti-cancer activity.

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