2762-59-6

Basic information

• Product Name: N-PHENYL-1-PIPERIDINECARBOTHIOAMIDE
• Synonyms: N-PHENYL-1-PIPERIDINECARBOTHIOAMIDE;N-Phenylpiperidine-1-carbothioamide;α-(Phenylimino)-1-piperidinemethanethiol
• CAS NO: 2762-59-6
• Molecular Formula: C₁₂H₁₆N₂S
• Molecular Weight: 220.33384
• Mol File: 2762-59-6.mol
• Article Data: 20

Chemical Properties

• Boiling Point: 326.3°Cat760mmHg
• Flash Point: 151.1°C
• Appearance: /
• Density: 1.197g/cm³
• Vapor Pressure: 0.000218mmHg at 25°C
• Refractive Index: 1.656
• CAS DataBase Reference: N-PHENYL-1-PIPERIDINECARBOTHIOAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-PHENYL-1-PIPERIDINECARBOTHIOAMIDE(2762-59-6)
• EPA Substance Registry System: N-PHENYL-1-PIPERIDINECARBOTHIOAMIDE(2762-59-6)

Safety Data

• Hazardous Substances Data: 2762-59-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H16N2S/c15-12(14-9-5-2-6-10-14)13-11-7-3-1-4-8-11/h1,3-4,7-8H,2,5-6,9-10H2,(H,13,15)

Upstream product

• 110-89-4 piperidine 
• 103-72-0 phenyl isothiocyanate 
• 62-53-3 aniline 
• 103-70-8 Formanilid 
• 92147-65-4 tert-butyl phenylcarbamodithioate 
• 1197040-29-1 phenyl isocyanate 
• 43009-16-1 phenyldithiocarbamic acid triethylamine salt 
• 75-15-0 carbon disulfide 
• 94-37-1 bis(piperidinothiocarbonyl)disulfide 

Downstream Products

• 110-89-4 piperidine 
• 102-08-9 N,N-diphenylthiourea 
• 132361-43-4 6-piperidino-2-trifluoromethyl-2,5-diphenyl-2H-1,3,5-thiadiazin-5-io-4-olate 
• 138761-12-3 C₂₁H₂₅N₃O₂S₃ 
• 132361-44-5 2-(4-methylphenyl)-6-piperidino-2-trifluoromethyl-5-phenyl-2H-1,3,5-thiadiazin-5-io-4-olate 
• 134720-39-1 4-Fluoro-N-phenyl-N-(piperidine-1-carbothioyl)-benzamide 
• 134720-38-0 3-Chloro-N-phenyl-N-(piperidine-1-carbothioyl)-benzamide 
• 134720-41-5 3,4,5-Trimethoxy-N-phenyl-N-(piperidine-1-carbothioyl)-benzamide 
• 134720-37-9 N-Phenyl-N-(piperidine-1-carbothioyl)-benzamide 
• 134720-36-8 (E)-3,N-Diphenyl-N-(piperidine-1-carbothioyl)-acrylamide 
• 134720-40-4 3,4-Dimethoxy-N-phenyl-N-(piperidine-1-carbothioyl)-benzamide 
• 2645-36-5 1-(N-phenylcarbamoyl)piperidine 
• 1422367-35-8 N₁-piperidine-N₂-phenyl biguanide hydrochloride 
• 2851-08-3 2-(piperidin-1-yl)benzo[d]thiazole 

Relevant articles and documents

Method for preparing aryl isothiourea

The invention discloses a method for preparing aryl isothiourea, wherein hydride is suspended in a solvent, and thiourea is sequentially added. O diiodo benzene followed by reaction to prepare aryl isothiosemicarbazone. The isothiourea structure is widely

An isocyanide based multi-component reaction under catalyst- and solvent-free conditions for the synthesis of unsymmetrical thioureas

A new and efficient method for the synthesis of thiourea derivatives by a sequential one-pot, three-component reaction between aromatic isocyanides, amines, and 1,2-di-tert-butyldisulfane (DTBS) was developed and 27 different examples were synthesized in good to excellent yields. DTBS was identified as an effective sulfur surrogate without the use of both catalysts and solvents. This protocol does not employ any transition metal catalyst or special experimental setup.

A highly efficient one-pot method for the synthesis of thioureas and 2-imino-4-thiazolidinones under microwave conditions

A one-pot synthesis of symmetrical and unsymmetrical substituted thioureas and 2-imino-4-thiazolidinones from simple starting materials under microwave irradiation and solventless conditions without base additives is presented. Various di- and trisubstituted thioureas are obtained in good yields in a few minutes. The sequential, three-component, one-pot synthesis of 2-imino-4-thiazolidinone derivatives is also studied, with satisfactory results obtained.