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2,4-Pentanedithiol, also known as 2,4-dimercaptopentane, is an organic compound characterized by the chemical formula C5H12S2. It is a colorless liquid with a strong, unpleasant odor. This chemical is composed of a five-carbon chain with two thiol (-SH) groups attached at the second and fourth carbon atoms. 2,4-Pentanedithiol is primarily used as a synthetic intermediate in the production of various chemicals, including pharmaceuticals, agrochemicals, and rubber chemicals. It is also employed as a reagent in organic synthesis and as a chain transfer agent in polymerization processes. Due to its reactive thiol groups, 2,4-pentanedithiol can form metal complexes and has potential applications in metal extraction and recovery.

4038-08-8

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4038-08-8 Usage

Usage

Building block for the synthesis of various organic compounds

Application

Reagent in organic chemistry reactions

Physical property

Strong odor

Industrial use

Production of flavors and fragrances

Role

Cross-linking agent in polymerization reactions

Function

Stabilizer in certain formulations

Chemical property

Metal chelating properties

Medical use

Treatment of heavy metal poisoning

Diverse applications

Across different industries due to unique chemical properties

Check Digit Verification of cas no

The CAS Registry Mumber 4038-08-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,3 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4038-08:
(6*4)+(5*0)+(4*3)+(3*8)+(2*0)+(1*8)=68
68 % 10 = 8
So 4038-08-8 is a valid CAS Registry Number.

4038-08-8Upstream product

4038-08-8Relevant academic research and scientific papers

Chiral oxazoline-1,3-dithianes: New effective nitrogen-sulfur donating ligands in asymmetric catalysis

Capito, Elena,Bernardi, Luca,Comes-Franchini, Mauro,Fini, Francesco,Fochi, Mariafrancesca,Pollicino, Salvatore,Ricci, Alfredo

, p. 3232 - 3240 (2005)

A series of new chiral oxazoline-1,3-dithianes has been easily synthesized and used as ligands for asymmetric catalysis. The conjugate addition of Et 2Zn to enones resulted in ees of up to 69%, whereas the Pd-catalyzed allylic alkylation led to

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