89652-23-3

Basic information

• Product Name: 2(1H)-Isoquinolinecarbothioamide, 3,4-dihydro-N-phenyl-
• Synonyms: 3,4-Dihydro-1H-isochinolin-2-thiocarbonsaeure-anilid;3,4-dihydro-1H-isoquinoline-2-carbothioic acid phenylamide;3,4-dihydro-1H-isoquinoline-2-carbothioic acid anilide
• CAS NO: 89652-23-3
• Molecular Formula: C16H16N2S
• Molecular Weight: 268.382
• Mol File: 89652-23-3.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2(1H)-Isoquinolinecarbothioamide, 3,4-dihydro-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(1H)-Isoquinolinecarbothioamide, 3,4-dihydro-N-phenyl-(89652-23-3)
• EPA Substance Registry System: 2(1H)-Isoquinolinecarbothioamide, 3,4-dihydro-N-phenyl-(89652-23-3)

Safety Data

• Hazardous Substances Data: 89652-23-3(Hazardous Substances Data)

Upstream product

• 91-21-4 1,2,3,4-tetrahydroisoquinoline 
• 1197040-29-1 phenyl isocyanate 
• 43009-16-1 phenyldithiocarbamic acid triethylamine salt 
• 103-72-0 phenyl isothiocyanate 
• 2744-08-3 decahydroisoquinoline 

Downstream Products

• 134720-54-0 N-(3,4-Dihydro-1H-isoquinoline-2-carbothioyl)-4-methyl-N-phenyl-benzamide 
• 134720-53-9 N-(3,4-Dihydro-1H-isoquinoline-2-carbothioyl)-N-phenyl-benzamide 
• 134720-55-1 Thiophene-2-carboxylic acid (3,4-dihydro-1H-isoquinoline-2-carbothioyl)-phenyl-amide 

Relevant articles and documents

Three-component reaction between isocyanides, aliphatic amines and elemental sulfur: Preparation of thioureas under mild conditions with complete atom economy

The reaction of isocyanides with aliphatic amines in the presence of elemental sulfur was found to proceed efficiently at, or near, room temperature to produce thioureas in excellent yields and with complete atom economy.

Heterocycle formation via palladium-catalyzed intramolecular oxidative C-H bond functionalization: An efficient strategy for the synthesis of 2-aminobenzothiazoles

N-Arylthioureas are converted to 2-aminobenzothiazoles via Intramolecular C-S bond formation/C-H functionalization utilizing an unusual cocatalytic Pd(PPh3)4MnO2 system under an oxygen atmosphere at 80 °C. This method elim

Fluorous electrophilic scavengers for solution-phase parallel synthesis

A fluorous isatoic anhydride and isocyanate are synthesized and used as scavengers for amines in solution-phase parallel synthesis of urea, thiourea, and β-hydroxyamine analogs. The resulting fluorous derivatives are readily separated from the reaction mi