15874-80-3

Basic information

• Product Name: Benzene, [(3-methyl-2-butenyl)sulfonyl]-
• CAS NO: 15874-80-3
• Molecular Formula: C11H14O2S
• Molecular Weight: 210.297
• Mol File: 15874-80-3.mol
• Article Data: 43

Chemical Properties

• CAS DataBase Reference: Benzene, [(3-methyl-2-butenyl)sulfonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(3-methyl-2-butenyl)sulfonyl]-(15874-80-3)
• EPA Substance Registry System: Benzene, [(3-methyl-2-butenyl)sulfonyl]-(15874-80-3)

Safety Data

• Hazardous Substances Data: 15874-80-3(Hazardous Substances Data)

Upstream product

• 15543-64-3 prenyl tolyl sulfone 
• 72863-21-9 (dimethyl-1,1 propene-2 yl) sulfonyl-1 methyl-4 benzene 
• 618-41-7 Benzenesulfinic acid 
• 10276-04-7 3-methyl-1-phenylsulfanylbut-2-ene 
• 591-50-4 iodobenzene 
• 90020-41-0 (1E)-3-methylbut-1-en-1-yl phenyl sulfone 
• 72863-20-8 α,α-Dimethylallyl phenyl sulfone 
• 873-55-2 sodium benzenesulfonate 
• 164513-96-6 1,1-dimethyl-2-propenyl isobutyl carbonate 
• 3017-69-4 2-methyl-1-propenylbromide 
• 3112-85-4 methylphenylsulfonate 
• 6110-01-6 4-phenylsulfanyl-butan-2-one 
• 24731-39-3 4-(phenylsulfonyl)butan-2-one 
• 108-98-5 thiophenol 

Downstream Products

• 68470-86-0 5-Benzenesulfonyl-2,7-dimethyl-octa-2,6-dien-4-one 
• 1071175-48-8 4-Benzenesulfonyl-3,3,6-trimethyl-hept-5-enoic acid ethyl ester 
• 97-41-6 ethyl trans-(+/-)-chrysanthemate 
• 84602-86-8 2-methyl-4-(phenylsulphonyl)-2-hexene 
• 78828-39-4 3-(1-Benzenesulfonyl-3-methyl-but-2-enyl)-cyclohexanone 
• 74866-54-9 2-methyl-4-(phenylsulfonyl)-(E)-2-octene 
• 68560-64-5 2-methyl-4-(phenylsulfonyl)dec-2-ene 
• 88958-92-3 4-(1-Benzenesulfonyl-3-methyl-but-2-enyl)-1-nitro-2-phenylsulfanyl-benzene 
• 128084-60-6 Trimethyl-((E)-4-methyl-1-phenethyl-penta-1,3-dienyloxy)-silane 
• 74866-36-7 2-Benzenesulfonyl-3,3-dimethyl-pent-4-enoic acid methyl ester 
• 68800-47-5 2-Benzenesulfonyl-5-methyl-hex-4-enoic acid methyl ester 
• 81635-12-3 (2,2-Difluoro-3,3-dimethyl-cyclopropylmethanesulfonyl)-benzene 
• 116883-28-4 1,4-dibenzyloxy-2,3-dimethoxy-5-methyl-6-(37'-phenylsulfonyl-3',7',11',15',19',23',27',31',35',39'-decamethyltetraconta-2'E,6'E,10'E,14'E,18'E,22'E,26'E,30'E,34'E,38'-decaenyl)benzene 
• 132407-53-5 (3R)-9-phenylsulfonyl nerolidol TBDMS ether 

Relevant articles and documents

-

-

Development of a new air-stable structure-simplified nafuredin-γ analog as a potent and selective nematode complex I inhibitor

Nafuredin-γ, obtained from natural nafuredin, has demonstrated a potent and selective inhibitory activity against nematode complex I. However, nafuredin-γ is unstable in air since its conjugated dienes are oxygen-labile. The instability in air was natural

CHINONE-, HYDROCHINOME- AND NAPHTHOCHINONE-ANALOGUES OF VATIQUIONE FOR TREATMENT OF MITOCHONDRIAL DISORDER DISEASES

The disclosure provides therapeutic compositions (i.e., therapeutic agents) and methods of preventing or treating Friedreich's ataxia in a mammalian subject, reducing risk factors, signs and/or symptoms associated with Friedreich's ataxia (e.g. Complex I deficiency), and/or reducing the likelihood or severity of Friedreich's ataxia. The disclosure further provides novel intermediates for the production of said therapeutic compositions and related reduced versions of said therapeutic compositions, which reduce forms may also be used as therapeutic agents (or prodrugs of the therapeutic agent(s)).

Silyloxymethanesulfinate as a sulfoxylate equivalent for the modular synthesis of sulfones and sulfonyl derivatives

An efficient protocol for the modular synthesis of sulfones and sulfonyl derivatives has been developed utilizing sodium tert-butyldimethylsilyloxymethanesulfinate (TBSOMS-Na) as a sulfoxylate (SO22-) equivalent. TBSOMS-Na, easily prepared from the commercial reagents Rongalite and TBSCl, serves as a potent nucleophile in S-alkylation and Cu-catalyzed S-arylation reactions with alkyl and aryl electrophiles. The sulfone products thus obtained can undergo the second bond formation at the sulfur center with various electrophiles without a separate unmasking step to afford sulfones and sulfonyl derivatives such as sulfonamides and sulfonyl fluorides.