3774-52-5

Basic information

• Product Name: 4-HYDROXYPHENYL THIOCYANATE
• Synonyms: 4-HYDROXYPHENYL THIOCYANATE;4-Thiocyanatophenol;4-Thiocyanophenol;p-Thiocyanatophenol;Thiocyanic acid 4-hydroxyphenyl ester
• CAS NO: 3774-52-5
• Molecular Formula: C₇H₅NOS
• Molecular Weight: 151.19
• Mol File: 3774-52-5.mol
• Article Data: 35

Chemical Properties

• Boiling Point: 309.1°C at 760 mmHg
• Flash Point: 140.8°C
• Appearance: /
• Density: 1.35g/cm³
• Vapor Pressure: 0.000358mmHg at 25°C
• Refractive Index: 1.654
• CAS DataBase Reference: 4-HYDROXYPHENYL THIOCYANATE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-HYDROXYPHENYL THIOCYANATE(3774-52-5)
• EPA Substance Registry System: 4-HYDROXYPHENYL THIOCYANATE(3774-52-5)

Safety Data

• Hazardous Substances Data: 3774-52-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H5NOS/c8-5-10-7-3-1-6(9)2-4-7/h1-4,9H

Upstream product

• 2987-46-4 4-thiocyanatoaniline 
• 56-23-5 tetrachloromethane 
• 5961-98-8 thiocyanatochloride 
• 108-95-2 phenol 
• 505-14-6 thiocyanogen 
• 333-20-0 potassium thioacyanate 
• 540-72-7 sodium thiocyanide 
• 1147550-11-5 ammonium thiocyanate 
• 28241-61-4 ammonia thiocyanic acid 
• 592-87-0 lead(II) thiocyanate 
• 637-89-8 4-sulfanylphenol 
• 859214-49-6 2-cyano-4-chloro-5-methoxypyridazin-3(2H)-one 
• 859214-48-5 2-cyano-4,5-dichloropyridazin-3(2H)-one 
• 75-52-5 nitromethane 

Downstream Products

• 15015-57-3 bis(4-hydroxyphenyl)disulfide 
• 637-89-8 4-sulfanylphenol 
• 89641-98-5 2-Nitro-4-thiocyanato-phenol 
• 5285-90-5 4-thiocyanatoanisole 
• 6860-75-9 Vinylsulfonsaeure-(4-thiocyanato-phenylester) 
• 83038-52-2 p-thiocyanatophenyl p'-decylbenzoate 
• 83038-50-0 p-thiocyanatophenyl p'-nonyloxybenzoate 
• 83038-48-6 p-thiocyanatophenyl p'-propyloxybenzoate 
• 83038-49-7 p-thiocyanatophenyl p'-pentyloxybenzoate 
• 404389-74-8 4-octyloxyphenyl thiocyanate 
• 102231-96-9 p-octyloxybenzenethiol 

Relevant articles and documents

N-Thiocyanato-2,10-camphorsultam Derivatives: Design and Applications of Original Electrophilic Thiocyanating Reagents

The synthesis of bench-stable electrophilic thiocyanating reagents was depicted in two steps from readily available starting materials in good yields. These newly designed electrophilic reagents were successfully applied for the thiocyanation of different

Selectfluor-initiated cyanation of disulfides to thiocyanates

A Selectfluor-initiated cyanation of disulfides to thiocyanates has been developed. In this process, Selectfluor was employed as the oxidant and trimethylsilyl cyanide was used as the cyanation reagent. It provides an eco-friendly and simple way to synthesize the thiocyanates.

ARS-TiO2 photocatalyzed direct functionalization of sp2 C-H bonds toward thiocyanation and cyclization reactions under visible light

An ARS-TiO2 photocatalyst has been prepared, by a simple method through stirring a mixture of ARS and TiO2 at room temperature in the dark, to extend the photocatalytic response of titanium dioxide toward the visible light spectrum. The synergic effect of ARS and TiO2 in the photocatalyst system has catalyzed direct C-H functionalization of sp2 C-H bonds toward thiocyanation and cyclization reactions. Several aromatic and heteroaromatic scaffolds (2-phenylamino-thiazole, phenol, aniline, indole and pyrrole derivatives) were treated with the thiocyanate anion at room temperature. Herein, the first report on thiocyanation of phenol and synthesis of 2-aminobenzothiazole derivatives under visible light is presented.