23566-17-8

Basic information

• Product Name: BIS(P-CHLOROBENZYL)DISULFIDE
• Synonyms: DI(4-CHLOROBENZYL) DISULFIDE;BIS(P-CHLOROBENZYL)DISULFIDE;Bis(4-chlorobenzyl) disulfide;NSC 190482
• CAS NO: 23566-17-8
• Molecular Formula: C₁₄H₁₂Cl₂S₂
• Molecular Weight: 315.28
• Mol File: 23566-17-8.mol
• Article Data: 39

Chemical Properties

• Melting Point: 59 °C
• Boiling Point: 420.9°Cat760mmHg
• Flash Point: 192.5°C
• Appearance: /
• Density: 1.342
• CAS DataBase Reference: BIS(P-CHLOROBENZYL)DISULFIDE(CAS DataBase Reference)
• NIST Chemistry Reference: BIS(P-CHLOROBENZYL)DISULFIDE(23566-17-8)
• EPA Substance Registry System: BIS(P-CHLOROBENZYL)DISULFIDE(23566-17-8)

Safety Data

• Hazardous Substances Data: 23566-17-8(Hazardous Substances Data)

Upstream product

• 104-83-6 1-Chloro-4-(chloromethyl)benzene 
• 81067-97-2 C₇H₆Cl₂S 
• 60-29-7 diethyl ether 
• 7732-18-5 water 
• 108881-33-0 S-(4-chlorobenzyl)benzothioate 
• 6258-66-8 (4-chlorophenyl)methanethiol 
• 491593-72-7 3,3-difluoro-1-iodo-2-phenyl-cyclopropene 
• 873-76-7 para-Chlorobenzyl alcohol 
• 68-12-2 N,N-dimethyl-formamide 
• 14752-65-9 sodium S-(4-chlorobenzyl) thiosulfate 
• 104-88-1 4-chlorobenzaldehyde 
• 594-42-3 chlorothio-trichloro-methane 
• 73447-15-1 μ-disulfido-1,2-dithio-dicarbonic acid O,O'-bis-(4-chloro-benzyl ester) 
• 2082-64-6 4-chlorobenzyl thiocyanate 

Downstream Products

• 2622-73-3 1-phenyl-2-(4-chlorophenyl)-1H-benzo[d]imidazole 
• 1450635-31-0 2-(4-chlorophenyl)-7-methoxythieno[3,2-b]pyridin-3-ol 
• 76625-89-3 p-chlorobenzyl α-disulfone 
• 99070-98-1 allyl 4-chlorobenzyl sulfide 
• 6265-91-4 2-(4-chlorophenyl)benzothiazole 
• 6966-45-6 4-chlorobenzylsulfonyl chloride 
• 5121-74-4 4,4'-dichlorostylbene 
• 2510-74-9 (E)-1,2-di(4-chlorophenyl)ethene 

Relevant articles and documents

Electrochemical α-thiolation and azidation of 1,3-dicarbonyls

A highly efficient electrochemical α-thiolation and azidation of 1,3-dicarbonyl compounds is developed. This electrochemical process is conducted under mild conditions without the use of a chemical oxidant, and exhibits a wide scope with good functional g

Trisulfides over disulfides: Highly selective synthetic strategies, anti-proliferative activities and sustained H2S release profiles

Temperature-and solvent-induced selective synthesis of trisulfides and disulfides is demonstrated. A remarkable selectivity was achieved using Na2S as a sulfur-Transfer agent under mild, greener, catalyst-free and additive-free conditions. This study reveals trisulfides as a better model than disulfides in general for a sustained release of H2S and potent anti-cancer activities.

Base-controlled Fe(Pc)-catalyzed aerobic oxidation of thiols for the synthesis of S-S and S-P(O) bonds

Fe(Pc)-Catalyzed aerobic oxidation of thiols for the synthesis of disulfides has been developed under mild reaction conditions. In addition, an aerobic oxidative cross-dehydrogenative coupling (CDC) reaction of thiols with P(O)-H compounds (H-phosphonates and H-phosphine oxide) for the formation of S-P(O) bonds has been demonstrated under the Fe(Pc) catalysis system with a base additive. Control experiments revealed that the use of a base (DIPA) in this system controls the synthetic pathways in which thiophosphates are formed.