128133-75-5

Basic information

• Product Name: benzyl-(3-bromophenyl)-sulfide
• Synonyms: benzyl-(3-bromophenyl)-sulfide
• CAS NO: 128133-75-5
• Molecular Weight: 279.2
• Mol File: 128133-75-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: benzyl-(3-bromophenyl)-sulfide(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl-(3-bromophenyl)-sulfide(128133-75-5)
• EPA Substance Registry System: benzyl-(3-bromophenyl)-sulfide(128133-75-5)

Safety Data

• Hazardous Substances Data: 128133-75-5(Hazardous Substances Data)

Upstream product

• 6320-01-0 3-Bromothiophenol 
• 100-44-7 benzyl chloride 
• 1207372-96-0 o-[2-(4-methoxyphenyl)ethynyl]benzoic acid benzyl ester 
• 100-39-0 benzyl bromide 

Downstream Products

• 1423146-01-3 benzyl(2'-fluoro-4'-methyl-5'-((2,2,2-trifluoroethyl)thio)-[1,1'-biphenyl]-3-yl)sulfane 
• 1459725-24-6 (E)-4-(N,N-diphenylamino)-3’-(benzylthio)stilbene 
• 1459725-33-7 (E)-(3-(4-(N,N-diphenylamino)styryl)phenyl)benzylmethylsulfonium trifluoromethanesulfonate 
• 1332344-46-3 C₁₄H₁₅BO₂S 
• 1332344-47-4 C₁₆H₂₁BO₂SSi 
• 325703-95-5 C₁₅H₁₂O₄S 
• 1221446-39-4 C₁₆H₁₂O₆S 
• 10490-07-0 2-phenyl-2-(phenylthio)acetic acid 
• 1204677-87-1 N-cyano-S-benzyl-S-(3-bromophenyl)sulfilimine 
• 94306-39-5 [1,1'-biphenyl]-3-yl(benzyl)sulfane 
• 406724-67-2 3-benzylthiotriphenylamine 

Relevant articles and documents

Design of D-π-A type photoacid generators for high efficiency excitation at 405 nm and 800 nm

New sulfonium salts with diphenylamino asymmetrically substituted stilbene as a D-π-A conjugated system have been synthesized. The resulting photoacid generators exhibit a highly efficient acid photogeneration process by either one-photon 405 nm or two-ph

SULPHUR-LINKED COMPOUNDS FOR TREATING OPHTHALMIC DISEASES AND DISORDERS

Provided are sulphur-linked compounds, pharmaceutical compositions thereof, and methods of treating ophthalmic diseases and disorders, such as age-related macular degeneration and Stargardt's Disease, using said compounds and compositions.

Synthesis of aryl benzyl NH-sulfoximines

Efficient synthesis and characterisation of a series of aryl benzyl NH-sulfoximines are described. While N-protected versions of aryl benzyl sulfoximines have been previously described, reports of their deprotection are very limited, presumably due to lab