151389-59-2

Basic information

• Product Name: N1-(2-BROMOETHYL)-4-CHLOROBENZENE-1-SULFONAMIDE, TECH
• Synonyms: N1-(2-BROMOETHYL)-4-CHLOROBENZENE-1-SULFONAMIDE, TECH;N-(2-bromoethyl)-4-chlorobenzenesulfonamide
• CAS NO: 151389-59-2
• Molecular Formula: C₈H₉BrClNO₂S
• Molecular Weight: 298.58456
• Mol File: 151389-59-2.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N1-(2-BROMOETHYL)-4-CHLOROBENZENE-1-SULFONAMIDE, TECH(CAS DataBase Reference)
• NIST Chemistry Reference: N1-(2-BROMOETHYL)-4-CHLOROBENZENE-1-SULFONAMIDE, TECH(151389-59-2)
• EPA Substance Registry System: N1-(2-BROMOETHYL)-4-CHLOROBENZENE-1-SULFONAMIDE, TECH(151389-59-2)

Safety Data

• Hazardous Substances Data: 151389-59-2(Hazardous Substances Data)

Upstream product

• 107-09-5 2-bromoethylamine 
• 98-60-2 4-chlorobenzenesulfonyl chloride 
• 2576-47-8 2-bromoethylamine hydrobromide 

Downstream Products

• 645393-23-3 N-(2-bromoethyl)-N-(1-ethoxycarbonyl)-4-chlorobenzenesulfonamide 
• 50707-38-5 N-(4-chlorophenylsulphonyl)aziridine 
• 645393-52-8 C₁₄H₁₇BrClNO₆S 
• 6318-34-9 N-ethyl-4-chlorobenzenesulfonamide 
• 645393-28-8 6-chloro-3,4-dihydro-2H-benzo[e][1,2]thiazine 1,1-dioxide 
• 141286-68-2 methyl 4-[2-(4-chlorophenylsulfonylamino)ethylthio]-2,6-difluorophenoxyacetate 
• 151389-60-5 4-Chloro-N-[2-(3,5-difluoro-4-hydroxy-phenylsulfanyl)-ethyl]-benzenesulfonamide 
• 169298-35-5 4-<2-(4-chlorophenylsulfonylamino)ethylthio>-2-fluorophenol 

Relevant articles and documents

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Carbazole-Containing Sulfonamides as Cryptochrome Modulators

The subject matter herein is directed to carbazole-containing sulfonamide derivatives and pharmaceutically acceptable salts or hydrates thereof of structural formula I wherein the variable R1, R2, R3, R4, R5, R6, R7, A, B, C, D, E, F, G, H, a, and b are accordingly described. Also provided are pharmaceutical compositions comprising the compounds of formula I to treat a Cry-mediated disease or disorder, such as diabetes, obesity, metabolic syndrome, Cushing's syndrome, and glaucoma.

Smiles-type free radical rearrangement of aromatic sulfonates and sulfonamides: Syntheses of arylethanols and arylethylamines

Smiles-type free radical rearrangements of arenesulfonates and arenesulfonamides are exploited for synthetic purposes. 4-Substituted benzenesulfonates cause Smiles-type rearrangement only when substituted by an electron withdrawing group. Therefore, ipso-sttack by an alkyl radical on arenesulfonates takes place in an electrophilic manner. Arenesulfonamides rearrange only when the amide nitrogen is substituted by an alkoxycarbonyl group, due to the electron withdrawing nature of this group. Sulfonates and the N-ethoxycarbonylsulfonamide derivatives of naphthalene, quinoline, and thiophene cause more rearrangement and show synthetic utility. Aromatic amino acid analogues were synthesized by Smiles-type rearrangement with moderate yields. The radical Smiles-type rearrangement of sulfonate and sulfonamide derivatives can be a useful synthetic route when we understand the electronic character of these reactions.