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Acetic acid, 2-(3,4-diphenyl-2(3H)-thiazolylidene)-, ethyl ester, also known as 2-(3,4-diphenyl-2(3H)-thiazolylidene)acetic acid ethyl ester, is a chemical compound with the molecular formula C19H17NO2S. It is a derivative of acetic acid, featuring a 3,4-diphenyl-2(3H)-thiazolylidene moiety attached to the acetic acid backbone. Acetic acid, 2-(3,4-diphenyl-2(3H)-thiazolylidene)-, ethyl ester is an organic ester, specifically an ethyl ester, and is characterized by its yellow crystalline appearance. It is used in various applications, including as an intermediate in the synthesis of pharmaceuticals and dyes, and as a reagent in chemical research. The compound is known for its stability and is often used in the preparation of other complex organic molecules.

7171-43-9

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7171-43-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7171-43-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,7 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7171-43:
(6*7)+(5*1)+(4*7)+(3*1)+(2*4)+(1*3)=89
89 % 10 = 9
So 7171-43-9 is a valid CAS Registry Number.

7171-43-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(3,4-diphenyl-1,3-thiazol-2-ylidene)acetate

1.2 Other means of identification

Product number -
Other names 2-(ethoxycarbonylmethylene)-2,3-dihydro-3,4-diphenylthiazole

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7171-43-9 SDS

7171-43-9Downstream Products

7171-43-9Relevant academic research and scientific papers

Utilization of α-halocarbonyl compounds in the synthesis of thiazole, thiadiazole, and thiophene derivatives

Abdel-Latif, Ehab,Bondock, Samir

, p. 299 - 305 (2006)

The behavior of ethyl 2-phenylthiocarbamoyl acetate 1 toward a variety of several α-halocarbonyl compounds was investigated. Thus, reaction of 1 with α-bromoketones, hydrazonoyl bromides, and 2-chloro-N-arylacetamides afforded the corresponding dihydrothi

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