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3-(4-chlorophenoxyacetyl)-thiazolidine-2-thione is a chemical compound with the molecular formula C10H8ClNO2S2. It is a derivative of thiazolidine-2-thione, featuring a 4-chlorophenoxyacetyl group attached to the 3-position of the thiazolidine ring. 3-(4-chlorophenoxyacetyl)-thiazolidine-2-thione is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the development of new drugs and pesticides. Its structure allows for further functionalization and modification, making it a versatile intermediate in organic chemistry. The presence of the chlorine atom in the phenoxyacetyl group can also facilitate reactions such as nucleophilic substitutions, which are common in the synthesis of complex molecules.

123529-83-9

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123529-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123529-83-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,5,2 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 123529-83:
(8*1)+(7*2)+(6*3)+(5*5)+(4*2)+(3*9)+(2*8)+(1*3)=119
119 % 10 = 9
So 123529-83-9 is a valid CAS Registry Number.

123529-83-9Relevant academic research and scientific papers

SUGAR CHEMISTRY WITHOUT PROTECTING GROUPS-III. A FACILE CHEMICAL SYNTHESIS OF 6-O-ACYL-D-GLYCOPYRANOSES AND METHYL-6-O-ACYL-D-GLYCOPYRANOSIDES.

Baczko, Krystyna,Plusquellec, Daniel

, p. 3817 - 3828 (1991)

Regioselective acylation of non protected glycopyranosides was performed using 3-acylthiazolidine-2-thiones 1 and the novel 3-acyl-5-methyl-1,3,4-thiadiazole-2(3H)-thiones 2 as the acylating reagents, yielding 6-O-acylated derivatives in high yields.Acyla

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