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Trans-5-phenyl-4-methyl-1,3-thiazolidine-2-thione is a chemical compound with the molecular formula C10H11NOS2. It is a derivative of 1,3-thiazolidine-2-thione, featuring a phenyl group at the 5th position and a methyl group at the 4th position. This organic compound is characterized by its thiazolidine ring structure, which consists of a sulfur atom, a nitrogen atom, and two carbon atoms. The trans configuration indicates that the phenyl and methyl groups are positioned on opposite sides of the double bond connecting the carbon atoms. trans-5-phenyl-4-methyl-1,3-thiazolidine-2-thione may have potential applications in pharmaceuticals, agrochemicals, or as a building block in the synthesis of more complex molecules.

1630-31-5

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1630-31-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1630-31-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,3 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1630-31:
(6*1)+(5*6)+(4*3)+(3*0)+(2*3)+(1*1)=55
55 % 10 = 5
So 1630-31-5 is a valid CAS Registry Number.

1630-31-5Relevant academic research and scientific papers

STEREOCHEMICAL COURSE OF THE REACTION OF 2-HALOETHYL ISOTHIOCYANATES WITH NUCLEOPHILES. sTEREOSPECIFIC ROUTE TO 4,5-DISUBSTITUTED Δ2-THIAZOLINES AND THIAZOLIDINE-2-THIONES

Kniezo, Ladislav,Kristian, Pavol,Budesinsky, Milos,Havrilova, Katarina

, p. 717 - 728 (2007/10/02)

Diastereoisomeric 1-chloro-1-phenyl-2-isothiocyanatopropanes have been prepared.They reacted stereospecifically with CH3ONa, diethylamine, aniline and NaSH to give pure cis or trans-4,5-disubstituted Δ2-thiazolines and thiazolidine-2-thiones whose configuration was determined using the nuclear Overhauser effect.The preponderant conformation of diastereoisomeric 1-chloro-1-phenyl-2-isothiocyanatopropanes was estimated on the basis of coupling constants of vicinal protons.

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