Cas 1207671-54-2,ethyl 4-[2-(4-chlorophenyl)-2-oxoethoxy]-2-methylthiophene-3-carboxylate

1207671-54-2

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Basic information

Product Name: ethyl 4-[2-(4-chlorophenyl)-2-oxoethoxy]-2-methylthiophene-3-carboxylate
Synonyms: ethyl 4-[2-(4-chlorophenyl)-2-oxoethoxy]-2-methylthiophene-3-carboxylate
CAS NO:1207671-54-2
Molecular Formula:
Molecular Weight: 338.812
EINECS: N/A
Product Categories: N/A
Mol File: 1207671-54-2.mol
Article Data: 1

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: ethyl 4-[2-(4-chlorophenyl)-2-oxoethoxy]-2-methylthiophene-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 4-[2-(4-chlorophenyl)-2-oxoethoxy]-2-methylthiophene-3-carboxylate(1207671-54-2)
EPA Substance Registry System: ethyl 4-[2-(4-chlorophenyl)-2-oxoethoxy]-2-methylthiophene-3-carboxylate(1207671-54-2)

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: 1207671-54-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1207671-54-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,7,6,7 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1207671-54:
(9*1)+(8*2)+(7*0)+(6*7)+(5*6)+(4*7)+(3*1)+(2*5)+(1*4)=142
142 % 10 = 2
So 1207671-54-2 is a valid CAS Registry Number.

1207671-54-2Upstream product

2158-82-9 4-hydroxy-2-methyl-thiophene-3-carboxylic acid ethyl ester

1207671-54-2Downstream Products

1207671-65-5 ethyl 3-(4-chlorophenyl)-5-methylthieno[3,2-b]furan-6-carboxylate

1207671-54-2Relevant articles and documents

Efficient methods for the synthesis of thieno[3,2-b]thiophene and thieno[3,2-b]furan derivatives

Shirinian, Valerii Z.,Shimkin, Alexey A.,Tipikin, Stepan N.,Krayushkin, Mikhail M.

experimental part, p. 3803 - 3806 (2010/03/26)

A novel approach to the synthesis of thieno[3,2b]thiophenes and thieno[3,2-b]furans bearing various substituents from readily accessible starting materials has been developed. The methodology is based on C- and O-alkylation of ethyl 4-hydroxy-2methylthiop

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