4513-27-3

Basic information

• Product Name: N-(CHLORO-PHENYL-METHYLENE)-4-METHYL-BENZENESULFONAMIDE
• Synonyms: Benzimidoylchloride, N-(p-tolylsulfonyl)- (6CI,7CI,8CI); N-(p-Tolylsulfonyl)benzimidoylchloride; N-(a-Chlorobenzylidene)-p-toluenesulfonamide;N-Tosylbenzimidoyl chloride
• CAS NO: 4513-27-3
• Molecular Formula: C₁₄H₁₂ClNO₂S
• Molecular Weight: 293.7686
• Mol File: 4513-27-3.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 435.2°Cat760mmHg
• Flash Point: 217°C
• Appearance: /
• Density: 1.25g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.591
• CAS DataBase Reference: N-(CHLORO-PHENYL-METHYLENE)-4-METHYL-BENZENESULFONAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(CHLORO-PHENYL-METHYLENE)-4-METHYL-BENZENESULFONAMIDE(4513-27-3)
• EPA Substance Registry System: N-(CHLORO-PHENYL-METHYLENE)-4-METHYL-BENZENESULFONAMIDE(4513-27-3)

Safety Data

• Hazardous Substances Data: 4513-27-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H12ClNO2S/c1-11-7-9-13(10-8-11)19(17,18)16-14(15)12-5-3-2-4-6-12/h2-10H,1H3/b16-14+

Upstream product

• 51376-74-0 α-Hydroxyiminobenzyl-p-tolylsulfon 
• 21272-79-7 1-methyl-4-(nitro(phenyl)methylsulfonyl)benzene 
• 6971-74-0 N-benzoyl-p-toluenesulfonamide 
• 70-55-3 toluene-4-sulfonamide 
• 98-88-4 benzoyl chloride 

Downstream Products

• 113510-76-2 N-[N-(toluene-4-sulfonyl)-benzimidoyl]-anthranilic acid methyl ester 
• 41274-12-8 N-thiazol-2-yl-N'-(toluene-4-sulfonyl)-benzamidine 
• 41274-21-9 N-(6-methyl-benzothiazol-2-yl)-N'-(toluene-4-sulfonyl)-benzamidine 
• 58999-81-8 C₁₆H₁₅NO₃S₃ 
• 58999-83-0 C₁₉H₂₁NO₃S₃ 
• 58999-82-9 C₁₇H₁₇NO₃S₃ 
• 58999-76-1 C₁₉H₂₂N₂O₂S₃ 
• 10520-99-7 N-thiobenzoyl-p-toluenesulfonamide 
• 833-50-1 2-phenylbenzo[d]oxazole 
• 120393-39-7 1-tosyl-2,4-diphenyl-1-aza-1-buten-3-yne 
• 4115-22-4 N¹-phenyl-N²-(p-tolylsulfonyl)benzamidine 
• 6971-74-0 N-benzoyl-p-toluenesulfonamide 
• 4115-16-6 p-tolylsulfonylbenzamidine 
• 22158-84-5 N-(p-Toluolsulfonyl)-benzimidsaeure-methylester 

Relevant articles and documents

Synthesis of 2-Imidazolines via Palladium-Catalyzed Cyclization Reaction of 2,3-Allenyl Amines and Aryl Iodides

An effective method for the synthesis of polysubstituted 2-imidazoline derivatives via palladium-catalyzed cyclization of 2,3-allenyl amines with aryl iodides is described. This pure domino process allows the formation of new carbon-carbon and carbon-nitrogen bonds in a single synthetic operation.