19432-96-3

Basic information

• Product Name: Benzene, [(3-chloropropyl)sulfonyl]-
• CAS NO: 19432-96-3
• Molecular Formula: C9H11ClO2S
• Molecular Weight: 218.704
• Mol File: 19432-96-3.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzene, [(3-chloropropyl)sulfonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(3-chloropropyl)sulfonyl]-(19432-96-3)
• EPA Substance Registry System: Benzene, [(3-chloropropyl)sulfonyl]-(19432-96-3)

Safety Data

• Hazardous Substances Data: 19432-96-3(Hazardous Substances Data)

Upstream product

• 4911-65-3 3-chloropropyl phenyl sulfide 
• 24536-40-1 3-phenylthiopropanol 
• 930-69-8 sodium thiophenolate 
• 25062-90-2 3-phenylsulfonylpropanol 
• 873-55-2 sodium benzenesulfonate 
• 108-98-5 thiophenol 
• 13033-58-4 3-Chloropropyl Phenyl Sulfoxide 
• 49639-22-7 phenyl 3-hydroxypropyl sulfoxide 

Downstream Products

• 17637-57-9 (cyclopropylsulfonyl)benzene 
• 115005-54-4 1-[3-(1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dion-7-yl)-2-hydroxypropyl]-4-(3-phenylsulfonylpropyl)piperazine 
• 187161-39-3 1-(3-chloropropylsulfonyl)-3-nitrobenzene 
• 1421917-99-8 3-(3-chloropropylsulfonyl)aniline 
• 1421918-02-6 N-4-(5-chlorobenzo[d][1,3]dioxol-4-yl)-N-2-(3-(3-chloropropylsulfonyl)phenyl)pyrimidine-2,4-diamine 
• 1421918-03-7 N₄-(5-chlorobenzo[d][1,3]dioxol-4-yl)-N₂-(3-(3-iodopropylsulfonyl)phenyl)pyrimidine-2,4-diamine 
• 1421918-04-8 3-(3-(4-(5-chlorobenzo-[d][1,3]dioxol-4-ylamino)pyrimidin-2-ylamino)phenylsulfonyl)propyl4-methylbenzenesulfonate 
• 1421917-97-6 C₂₀H₁₈Cl⁽¹⁸⁾FN₄O₄S 
• 1229622-06-3 C₂₀H₂₅NO₄S 
• 1253197-31-7 (+/-)-7-benzyloxy-3-[3-(phenylsulfonyl)propyl]-2,3,4,5-tetrahydro-1H-3-benzazepin-1-ol 
• 886368-32-7 1-phenylsulfonyl-3-(phenylthio)propane 
• 112859-57-1 5-[1-[5-(3-Benzenesulfonyl-propoxy)-2-nitro-phenyl]-meth-(Z)-ylidene]-1-methyl-imidazolidine-2,4-dione 
• 112859-56-0 5-[1-[5-(3-Benzenesulfonyl-propoxy)-2-nitro-phenyl]-meth-(Z)-ylidene]-imidazolidine-2,4-dione 
• 112859-22-0 1,3-Dihydro-1-methyl-7-[3-(phenylsulfonyl)propoxy]-2H-imidazo[4,5-b]quinolin-2-one 

Relevant articles and documents

Synthesis of α-Cyano and α-Sulfonyl Cyclic Ethers via Intramolecular Reactions of Peroxides with Sulfone- And Nitrile-Stabilized Carbanions

The intramolecular reaction of carbon nucleophiles with oxygen-centered electrophiles has been little explored outside of nucleophilic epoxidation. We now report the synthesis of sulfonyl- and cyano-substituted oxacycles via intramolecular reaction of sul

Fluorine-18 Radiolabeling and Radiopharmacological Characterization of a Benzodioxolylpyrimidine-based Radiotracer Targeting the Receptor Tyrosine Kinase EphB4

Members of the Eph receptor tyrosine kinase family play essential roles in the pathogenesis of cancer and are therefore promising candidates for molecular imaging by positron emission tomography (PET), for example. In this regard, radiochemical access to

Synthesis and pharmacological properties of benzamide derivatives as selective serotonin 4 receptor agonists

A series of 4-amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamides with a polar substituent group at the 1-position of the piperidine ring was synthesized and evaluated for its effect on gastrointestinal motility. The benzoyl, phenylsulfonyl, and benzylsulfonyl derivatives accelerated gastric emptying and increased the frequency of defecation. One of them, 4-amino-N-[1-[3-(benzylsulfonyl)propyl]piperidin-4-ylmethyl]-5-chloro-2- methoxybenzamide (13a, Y-36912), was a selective 5-HT4 receptor agonist offering potential as a novel prokinetic with reduced side effects derived from 5-HT3- and dopamine D2 receptor-binding affinity. In the oral route of administration, this compound enhanced gastric emptying and defecation in mice, and has a possibility as a prokinetic agent, which is effective on both the upper and the lower gastrointestinal tract.