37755-03-6

Basic information

• Product Name: 3,3'-dinitrodiphenyl sulfide
• Synonyms: 3,3'-dinitrodiphenyl sulfide
• CAS NO: 37755-03-6
• Molecular Weight: 276.273
• Mol File: 37755-03-6.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 3,3'-dinitrodiphenyl sulfide(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3'-dinitrodiphenyl sulfide(37755-03-6)
• EPA Substance Registry System: 3,3'-dinitrodiphenyl sulfide(37755-03-6)

Safety Data

• Hazardous Substances Data: 37755-03-6(Hazardous Substances Data)

Upstream product

• 16278-29-8 3-nitrobenzenediazonium 
• 3814-18-4 3-nitrothiophenol 
• 645-00-1 m-iodonitrobenzene 
• 586-36-7 3-nitrophenyldiazonium tetrafluoroborate 
• 17356-08-0 thiourea 
• 62-55-5 thioacetamide 
• 537-91-7 bis(3-nitrophenyl) disulfide 

Downstream Products

• 92695-58-4 bis(3-nitrophenyl)sulfoxide 

Relevant articles and documents

High surface and magnetically recoverable mPANI/pFe3O 4 nanocomposites for C-S bond formation in water

A high surface area mPANI/pFe3O4 nanocomposite from mesoporous polyaniline and porous magnetic Fe3O4 was used as a catalyst in the S-arylation of thiophenol with aryl chlorides and in the C-S bond formation between aryl iodides and thiourea in water. The mesoporosity of the polyaniline enhances the efficiency and stability of the porous magnetic Fe3O4 nanoparticles in both coupling reactions. The mPANI/pFe3O4 nanocomposite can be recovered with an external magnet and reused several times due to the superparamagnetic nature of the porous Fe3O4 nanoparticles.

Spherical organic photoelectric material and preparation method and application thereof

The invention discloses a spherical organic photoelectric material and a preparation method and application thereof. The material is of a non-conjugated spherical shape; the left side and the right side are donor units; the middle is an acceptor unit; a c

Aryl diazonium salt and thioacetamide: A catalyst free, efficient blend of an inexpensive arylating agent with "s" surrogate for sulphide synthesis

Novel, facile C-S and S-S bond coupling reactions were achieved by using an aryl diazonium salt as an arylating agent and thioacetamide as a sulphur surrogate. The reaction proceeds smoothly at room temperature without using any transition metal catalyst, ligand or base. Aryl diazonium salts undergo rapid reactions with thioacetamide at room temperature to give the desired products in a much shorter period than the previously reported metal catalysed protocols.