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3-Thiophenecarboxylic acid, 4-hydroxy-2-phenyl, ethyl ester is a complex organic compound with the chemical formula C13H12O3S. It is derived from 3-thiophenecarboxylic acid, which is a heterocyclic compound containing a sulfur atom in the ring structure. The molecule features a 4-hydroxy-2-phenyl substitution pattern, where a hydroxyl group is attached to the 4th carbon of the thiophene ring, and a phenyl group is connected to the 2nd carbon. The ethyl ester functional group is formed by the esterification of the carboxylic acid with ethanol, resulting in an ethoxycarbonyl group. 3-Thiophenecarboxylic acid, 4-hydroxy-2-phenyl-, ethyl ester is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, as well as its role as an intermediate in various chemical reactions.

1022-06-6

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1022-06-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1022-06-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1022-06:
(6*1)+(5*0)+(4*2)+(3*2)+(2*0)+(1*6)=26
26 % 10 = 6
So 1022-06-6 is a valid CAS Registry Number.

1022-06-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-2-phenyl-3-thiophenecarboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 4-hydroxy-2-phenyl-thiophene-3-carboxylic acid ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:1022-06-6 SDS

1022-06-6Relevant academic research and scientific papers

RHODIUM(II) CATALYZED CYCLIZATION OF DIAZO THIOCARBONYL COMPOUNDS FOR HETEROCYCLIC SYNTHESIS

Padwa, Albert,Kinder, Frederic R.,Nadler, William R.,Zhi, Lin

, p. 367 - 383 (2007/10/02)

The mesoionic thioisomuenchnone system was prepared from the rhodium(II) acetate catalyzed cyclization of a diazothioamide and was found to undergo smooth 1,3-dipolar cycloaddition with N-phenylmaleimide.In contrast to this system, the rhodium(II) reaction of α-diazo-β-oxo ester containing a thiocarbonyl group produced a cyclic thiocarbonyl ylide which extruded sulfur from a transient episulfide intermediate.

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