6345-64-8

Basic information

• Product Name: Bis(4-iodophenyl) disulfide
• CAS NO: 6345-64-8
• Molecular Formula: C₁₂H₈I₂S₂
• Molecular Weight: 470.137
• Mol File: 6345-64-8.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Bis(4-iodophenyl) disulfide(CAS DataBase Reference)
• NIST Chemistry Reference: Bis(4-iodophenyl) disulfide(6345-64-8)
• EPA Substance Registry System: Bis(4-iodophenyl) disulfide(6345-64-8)

Safety Data

• Hazardous Substances Data: 6345-64-8(Hazardous Substances Data)

Upstream product

• 2516-96-3 2-chloro-5-nitrobenzoic acid 
• 52928-01-5 4-iodothiophenol 
• 2828-64-0 4-iodo-benzenesulfonic acid-anhydride 
• 722-27-0 bis(4-aminophenyl)disulfide 
• 3321-93-5 4-iodo-phenyl thiocyanate 
• 589-87-7 1,4-bromoiodobenzene 
• 1193-02-8 4-aminotiophenol 
• 7664-41-7 ammonia 
• 1514-50-7 4-iodobenzenediazonium tetrafluoroborate 
• 10387-40-3 potassium thioacetate 
• 98-61-3 p-Iodobenzenesulfonyl chloride 

Downstream Products

• 100329-63-3 C₁₂H₉ClINO₂S₂ 
• 52928-01-5 4-iodothiophenol 
• 1338595-39-3 (4-iodophenyl)(naphthalen-2-yl)sulfane 
• 100329-89-3 S-(2,2-diethoxyethyl)-S-p-iodophenyl-N-phenylsulfonylsulfimide 
• 100339-89-7 C₁₆H₁₇ClINO₃S₂ 

Relevant articles and documents

MATRIX METALLOPROTEINASE (MMP) INHIBITORS AND METHODS OF USE THEREOF

Hydantoin based compounds useful as inhibitors of matrix metalloproteinases (MMPs), particularly macrophage elastase (MMP-12) are described. Also described are related compositions and methods of using the compounds to inhibit MMP-12 and treat diseases mediated by MMP-12, such as asthma, chronic obstructive pulmonary disease (COPD), emphysema, acute lung injury, idiopathic pulmonary fibrosis (IPF), sarcoidosis, systemic sclerosis, liver fibrosis, nonalcoholic steatohepatitis (NASH), arthritis, cancer, heart disease, inflammatory bowel disease (IBD), acute kidney injury (AKI), chronic kidney disease (CKD), Alport syndrome, and nephritis.

Thieme Chemistry Journals Awardees - Where Are They Now?Molybdenum(V)-Mediated Synthesis of Nonsymmetric Diaryl and Aryl Alkyl Chalcogenides

Oxidative chalcogenation reaction using molybdenum(V) reagents provides fast access to a wide range of nonsymmetric aryl sulfides and selenides. The established protocol is tolerated by a variety of labile functions, protecting groups, and aromatic heterocycles. In particular, when labile moieties are present, the use of molybdenum(V) reagents provides superior yields compared to other oxidants.

Tunable and Practical Synthesis of Thiosulfonates and Disulfides from Sulfonyl Chlorides in the Presence of Tetrabutylammonium Iodide

A tunable and practical synthesis of electrophilic sulfenylating reagents, thiosulfonates and disulfides, from inexpensive and easily available sulfonyl chlorides, has been developed. By appropriate choice of solvents, the reaction of sulfonyl chlorides and tetrabutylammonium iodide gave the target products in good to excellent yields, respectively. These transformations probably proceed through a reducing–coupling pathway. (Figure presented.).