4426-82-8

Basic information

• Product Name: Benzene, (1-isothiocyanatopropyl)-
• CAS NO: 4426-82-8
• Molecular Formula: C10H11NS
• Molecular Weight: 177.27
• Mol File: 4426-82-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzene, (1-isothiocyanatopropyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (1-isothiocyanatopropyl)-(4426-82-8)
• EPA Substance Registry System: Benzene, (1-isothiocyanatopropyl)-(4426-82-8)

Safety Data

• Hazardous Substances Data: 4426-82-8(Hazardous Substances Data)

Upstream product

• 63615-82-7 (2-iodo-1-isothiocyanato-propyl)-benzene 
• 62559-30-2 1-phenylpropyl trimethylsilyl ether 
• 1147550-11-5 ammonium thiocyanate 
• 93-54-9 1-Phenyl-1-propanol 
• 540-72-7 sodium thiocyanide 
• 3674-54-2 tetrabutylammonium thiocyanate 
• 321884-15-5 2-(1-phenyl-propoxy)-tetrahydro-pyran 
• 2941-20-0 1-phenylpropylamine 
• 75-15-0 carbon disulfide 
• 463-71-8 thiophosgene 
• 333-20-0 potassium thioacyanate 

Downstream Products

• 131156-79-1 4-ethyl-4-phenylthiazolidine-2,5-dithione 
• 74787-82-9 1-(2-Methyl-allyl)-3-(1-phenyl-propyl)-thiourea 
• 74548-50-8 1-(3-Hydroxy-propyl)-3-(1-phenyl-propyl)-thiourea 
• 62466-37-9 N-phenyl-N'-(1-phenyl-propyl)-thiourea 
• 74548-42-8 1-(2-Hydroxy-ethyl)-3-(1-phenyl-propyl)-thiourea 
• 74787-84-1 1-(2-Hydroxy-ethyl)-1-methyl-3-(1-phenyl-propyl)-thiourea 

Relevant articles and documents

Multiple binding modes of isothiocyanates that inhibit macrophage migration inhibitory factor

Macrophage migration inhibitory factor (MIF) is a pleiotropic cytokine that has roles in the innate immune response, and also contributes to inflammatory disease. While the biological properties of MIF are closely linked to protein-protein interactions, M

Preparation of thiocyanates and isothiocyanates from alcohols, thiols, trimethylsilyl-, and tetrahydropyranyl ethers using triphenylphosphine/2,3-dichloro-5,6-dicyanobenzoquinone (DDQ)/n-Bu4NSCN system

A combination of triphenylphosphine (PPh3) and 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) provides a safe and easily available mixed reagent system for the conversion of 1° and 2° alcohols, thiols, trimethylsilyl-, and tetrahydropyranyl ethers to their corresponding thiocyanates and the 3° ones to isothiocyanates in good to high yields.

Efficient conversion of tetrahydropyranyl (THP) ethers to their corresponding thiocyanates with in-situ-generated Ph3P(SCN) 2

Immediate and efficient one-pot conversion of tetrahydropyranyl (THP) ethers to their corresponding thiocyanates by in-situ-generated Ph 3P(SCN)2 is described. Primary and secondary alkyls and also benzylic THP ethers are converted to their corresponding thiocyanates in excellent yields at room temperature by this method. Copyright Taylor & Francis Inc.