100726-99-6

Basic information

• Product Name: Benzene, 1-iodo-4-[(phenylsulfonyl)methyl]-
• CAS NO: 100726-99-6
• Molecular Formula: C13H11IO2S
• Molecular Weight: 358.2
• Mol File: 100726-99-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1-iodo-4-[(phenylsulfonyl)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-iodo-4-[(phenylsulfonyl)methyl]-(100726-99-6)
• EPA Substance Registry System: Benzene, 1-iodo-4-[(phenylsulfonyl)methyl]-(100726-99-6)

Safety Data

• Hazardous Substances Data: 100726-99-6(Hazardous Substances Data)

Upstream product

• 930-69-8 sodium thiophenolate 
• 624-31-7 4-tolyl iodide 
• 16004-15-2 1-bromomethyl-4-iodobenzene 
• 873-55-2 sodium benzenesulfonate 
• 100727-00-2 (4-iodo-benzyl)-phenyl sulfide 

Downstream Products

• 832744-33-9 1-bromo-4-(2-(4-iodophenyl)ethynyl)benzene 
• 947495-10-5 4-iodo(dithiobenzoic) acid 2-(trimethylsilyl)ethyl ester 
• 13041-71-9 (E)-1-(4-iodophenyl)-2-phenylethene 
• 1209009-05-1 1-iodo-4-(phenylbuta-1,3-diyn-1-yl) benzene 
• 1243693-93-7 1-(4-iodophenyl)-4-(4-diphenylaminophenyl)butadiyne 

Relevant articles and documents

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PF-543 has been known as a substance that strongly inhibits SK1. However, it also exhibits antineoplastic activity that is lower than other inhibitors of SK1. In this study, we compared PF-543 and synthesized a newly designed derivative of PF-543 (compoun

Double elimination protocol for convenient synthesis of dihalodiphenylacetylenes: Versatile building blocks for tailor-made phenylene-ethynylenes

Dihalodiphenylacetylenes are conveniently synthesized by a double elimination reaction of β-substituted sulfones which are readily obtained from halogen-substituted benzyl sulfone and benzaldehyde derivatives. Halogens can be incorporated at any desired positions in the diphenylacetylene skeleton simply by choosing the substitution position of the halogen on the aromatic rings of the starting compounds. The diphenylacetylenes with different halogen substituents thus obtained undergo sequential carbon-carbon bond formations due to the different reactivities of the halogens. Thus, various moieties can be incorporated on the diphenylacetylene skeleton at whichever positions so that a variety of tailor-made phenylene-ethynylenes with regulated structure and composition could be designed.