59293-67-3

Usage

Uses

Used in Pharmaceutical Industry:
2,4-Dichlorobenzyl mercaptan is used as a synthetic intermediate for the production of various pharmaceuticals. Its role in the synthesis process allows for the creation of a wide range of medicinal compounds that can address different health conditions.
Used in Pesticide Industry:
In the pesticide industry, 2,4-Dichlorobenzyl mercaptan is employed as a building block in the synthesis of various pesticides. Its incorporation into these chemical products contributes to the development of effective solutions for pest control in agriculture and other settings.
Used in Specialty Chemicals Production:
2,4-Dichlorobenzyl mercaptan is used as a key component in the production of specialty chemicals. Its unique properties enable the creation of customized chemical products that cater to specific industrial needs.
Used as a Reagent in Organic Synthesis:
2,4-Dichlorobenzyl mercaptan is utilized as a reagent in organic synthesis to introduce the 2,4-dichlorobenzyl group into organic molecules. This capability expands the range of possible chemical reactions and outcomes, facilitating advancements in the field of organic chemistry.

InChI:InChI=1/C7H6Cl2S/c8-6-2-1-5(4-10)7(9)3-6/h1-3,10H,4H2

Upstream product

• 188065-31-8 2,4-dichloro-1-{[(2,4-dichlorobenzyl)disulfanyl]methyl}benzene 
• 94-99-5 2,4-Dichlorobenzyl chloride 
• 17356-08-0 thiourea 
• 131887-63-3 [(2,4-Dichloro-benzylsulfanyl)-dimethylamino-methylene]-dimethyl-ammonium; iodide 
• 1777-82-8 (2,4-dichlorophenyl)methanol 
• 874-42-0 2,4-dichlorobenzaldeyhde 
• 72214-67-6 S-(2,4-dichlorobenzyl)isothiourea hydrochloride 
• 28249-28-7 dimethyl-dithiocarbamic acid-(2,4-dichloro-benzyl ester) 

Downstream Products

• 41022-54-2 ethyl 2-(2, 4-dichlorophenyl)acetate 
• 129789-64-6 5'-O-Dimethoxytritylthymidine-3'-O-[β-cyanoethyl-(S-2,4-dichlorobenzyl)]-phosphorodithioate 
• 119595-47-0 C₄₈H₄₇Cl₂N₄O₇PS 
• 116872-59-4 5'-O-tritylthymidine-3'-O(S-2,4 dichlorobenzylmethyl)methylphosphonothioate 
• 119595-46-9 C₄₂H₄₄Cl₂N₃O₇PS 
• 119595-51-6 C₄₉H₄₇Cl₂N₆O₆PS 
• 119595-55-0 C₄₆H₄₉Cl₂N₆O₇PS 
• 73024-13-2 17α-<(2,4-dichlorobenzyl)thio>-1,4-androstadiene-3,11-dione 
• 75663-55-7 4-(2-fluorophenyl)-1,2,3,6-tetrahydro-1-methylpyridine 
• 72364-69-3 4-(2,4-Dichloro-benzylsulfanyl)-4-(2-fluoro-phenyl)-1-methyl-piperidine 
• 119619-08-8 O-(5'-O-(dimethoxytrityl)thymidin-3'-yl) S-(2,4-dichlorobenzyl) N,N-dimethyl thiophosphoramidite 
• 119595-50-5 C₄₆H₄₅Cl₂N₄O₇PS 
• 119595-54-9 C₄₇H₄₅Cl₂N₆O₆PS 
• 119595-58-3 C₄₄H₄₇Cl₂N₆O₇PS 

Relevant academic research and scientific papers

Nonenzymatic Dynamic Kinetic Resolution of in situ Generated Hemithioacetals: Access to 1,3-Disubstituted Phthalans

The first nonenzymatic DKR reaction of hemithioacetals is developed. Hemithioacetals were formed in situ via thiol addition and subsequently underwent an intramolecular oxa-Michael reaction. The scope of the reaction was quite broad ranging from aliphatic to aromatic substituents and 1,3-disubstituted-1,3-dihyroisobenzofuran products were obtained in good yields with moderate diastereoselectivities and high enantioselectivities. (Figure presented.).

One pot rapid synthesis of thiols from alcohols under mild conditions

Thiols are prepared in high yields from corresponding alcohols using Ph3P, NBS in acetone and followed by addition of polymer supported hydrosulfide under mild condition.

Solid Supported Reagents and Reactions. Part 21.1 Rapid and Clean Synthesis of Thiols from Halides Using Polymer-supported Hydrosulfide

A variety of thiols are prepared from corresponding halides using polymer-supported hydrosulfide in excellent yields. Isolation of pure products by simple filtration and evaporation is an important feature of this method.

Sulfur-containing imidazoles

Novel imidazole mercaptals of the formula STR1 wherein each m is independently zero or one; and R1 and R2 each are independently selected from (lower)alkyl, cycloalkyl, cycloalkyl(lower)alkyl, phenyl, phenyl(lower)alkyl, thienyl, thienyl(lower)alkyl, pyridyl and pyridyl(lower)alkyl, in which the phenyl and heterocyclic rings optionally may contain from 1 to 3 substituents, and acid addition salts thereof, are useful antimicrobial agents.