5694-48-4

Upstream product

• 35128-29-1 4-bromomethyl-2-phenyl-[1,3]dithiolane 
• 14043-90-4 (+/-)-cis-4-(3,5-dinitro-benzoyloximethyl)-2-phenyl-[1,3]dithiolane 
• 59-52-9 2,3-dimercaptopropanol 
• 100-52-7 benzaldehyde 

Downstream Products

• 41159-21-1 2-Phenyl-4-chlormethyl-dithiolan 
• 35128-29-1 4-bromomethyl-2-phenyl-[1,3]dithiolane 
• 79130-15-7 Carbamic acid (2R,4R)-2-phenyl-[1,3]dithiolan-4-ylmethyl ester 
• 79130-16-8 Carbamic acid (2R,4R)-2-(4-chloro-phenyl)-[1,3]dithiolan-4-ylmethyl ester 
• 81546-92-1 4-p-toluenesulfonyloxymethyl-2-phenyl-1,3-dithiolane 
• 5694-46-2 4-mercaptomethyl-2-phenyl-[1,3]dithiolane 
• 107151-79-1 4-(3,5-dinitro-benzoyloximethyl)-2-phenyl-[1,3]dithiolane-1,1,3,3-tetraoxide 
• 5694-48-4 (+/-)-(cis-2-phenyl-[1,3]dithiolan-4-yl)-methanol 
• 100-53-8 phenylmethanethiol 
• 81546-93-2 9-((RS)-2-phenyl-1,3-dithiolane-4-ylmethyl)adenine 
• 14043-90-4 (+/-)-trans-4-(3,5-dinitro-benzoyloximethyl)-2-phenyl-[1,3]dithiolane 
• 14043-90-4 (+/-)-cis-4-(3,5-dinitro-benzoyloximethyl)-2-phenyl-[1,3]dithiolane 

Relevant academic research and scientific papers

Acrylic ester compound and usage thereof

An acrylic ester compound represented by the general formula (1): wherein, R1 and R2 represent independently a hydrogen atom, an alkyl group which may have a substituent, an aromatic alkyl group which may have a substituent or an aromatic residue which may have a substituent, respectively; R3 represents a hydrogen atom or an alkyl group; A represents a divalent organic group; and X represents a sulfur atom or an oxygen atom; provided that when X is an oxygen atom, R1 represents an aromatic residue that may have a substituent, a polymerizable composition comprising the compound, and a cured article and optical components obtained by polymerizing the polymerizable composition.

Acrylic ester compound and usage thereof

An acrylic ester compound represented by the general formula (1): wherein, R1 and R2 represent independently a hydrogen atom, an alkyl group which may have a substituent, an aromatic alkyl group which may have a substituent or an aro

Comparative radioprotective activity of various pentagonal compounds with two heteroatomes

Various heterocyclic compounds with two heteroatomes were synthesized and their potential radioprotective activity was tested. This study shows the interest of phenylthiazolidines derivatives in chemical radioprotection.

O-Ethyl-s-propyl derivatives of 1,3-dithiolan-4-yl phosphorodithioates-methyl

Compounds characterized by the following formula: SPC1 Wherein R and R' can be selected from the group consisting of C1 to C15 hydrocarbyl, preferably C1 to C6 alkyl, C3 to C7 cycloalkyl, phenyl optionally substituted by chlorine, bromine, nitro, cyano, C1 to C6 alkyl, C1 to C6 alkoxy or C1 to C6 alkylthio; R and R' may form together a carbocyclic ring of from 3 to 8 carbon atoms. In addition, R can also be hydrogen. R" can be a C1 to C6 alkyl group optionally substituted by chlorine, bromine or cyano; phenyl optionally substituted by chlorine, bromine or nitro, R"' can have the same definition as R" and can be in addition a C1 to C6 alkoxy, C1 to C4 alkylthio and phenoxy optionally substituted by chlorine, bromine or nitro; X can be oxygen or sulfur. These compounds have been found to possess pesticidal activity, particularly insecticidal, miticidal and nematocidal activity.