10151-96-9

Basic information

• Product Name: 2-[(4-methylphenyl)amino]-2-oxoethyl thiocyanate
• CAS NO: 10151-96-9
• Molecular Formula: C₁₀H₁₀N₂OS
• Molecular Weight: 206.2642
• Mol File: 10151-96-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 427.1°C at 760 mmHg
• Flash Point: 212.1°C
• Density: 1.268g/cm³
• Vapor Pressure: 1.68E-07mmHg at 25°C
• Refractive Index: 1.63
• CAS DataBase Reference: 2-[(4-methylphenyl)amino]-2-oxoethyl thiocyanate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(4-methylphenyl)amino]-2-oxoethyl thiocyanate(10151-96-9)
• EPA Substance Registry System: 2-[(4-methylphenyl)amino]-2-oxoethyl thiocyanate(10151-96-9)

Safety Data

• Hazardous Substances Data: 10151-96-9(Hazardous Substances Data)

Usage

General Description

2-[(4-methylphenyl)amino]-2-oxoethyl thiocyanate is a chemical compound with the molecular formula C10H10N2OS. It is a thiocyanate derivative with a substituted phenyl group and a ketone functional group. 2-[(4-methylphenyl)amino]-2-oxoethyl thiocyanate is used in various chemical reactions and synthesis processes. It may also have potential applications in pharmaceuticals, agrochemicals, and materials science. Additionally, it is important to handle this chemical with caution and use appropriate safety measures due to its potential hazards.

Upstream product

• 333-20-0 potassium thioacyanate 
• 16634-82-5 N-(p-tolyl)-2-chloroacetamide 
• 5343-65-7 2-bromo-N-p-tolylacetamide 
• 532-55-8 Benzoyl isothiocyanate 
• 1147550-11-5 ammonium thiocyanate 

Downstream Products

• 20579-81-1 2-imino-3-(4-methylphenyl)-4-thiazolidinone 

Relevant articles and documents

A convenient, rapid, and general synthesis of α-oxo thiocyanates using clay supported ammonium thiocyanate

A very rapid, convenient, and general method for the synthesis of α-oxo thiocyanates has been described by using clay supported ammonium thiocyanate. The procedure avoids the use of additional catalyst, solvent, aqueous work-up and the yields are high. Moreover, the method is applicable for a variety of aryl, heteroaryl, alkyl α-halo carbonyls, β-keto tosylates, α-halo β-dicarbonyl, α-tosyl, β-dicarbonyl, alkyl halide, and alkyl tosylates.

Production of carbonyl compounds substituted in α-position

Production of carbonyl compounds substituted in the α-position and having the formula: EQU1 wherein R1 is alkyl, aralkyl, phenyl, toluyl, naphthyl, alkoxy or amino; R2 is hydrogen EQU2 A is hydrogen, alkyl, halo or EQU3 R6 is hydrogen or methyl, and R11 is alkyl; wherein said compounds are formed by reacting a sulfur ylide having the formula: EQU4 wherein Y is the radical EQU5 and R9 and R10 are alkyl or phenyl, with a solution containing both an electrophilic agent A' that is converted into the radical A and a nucleophilic agent B' that is converted into the radical B. The resulting carbonyl compounds are useful as starting materials for the production of paper, textile, and leather auxiliaries, plant protection agents, alkyd resins, polyesters and polyamides.