62380-38-5

Basic information

• Product Name: phenyl (3-hydroxyphenyl)carbamate
• CAS NO: 62380-38-5
• Molecular Formula: C₁₃H₁₁NO₃
• Molecular Weight: 229.2313
• Mol File: 62380-38-5.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 372.2°C at 760 mmHg
• Flash Point: 178.9°C
• Density: 1.326g/cm³
• Vapor Pressure: 4.57E-06mmHg at 25°C
• Refractive Index: 1.662
• CAS DataBase Reference: phenyl (3-hydroxyphenyl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl (3-hydroxyphenyl)carbamate(62380-38-5)
• EPA Substance Registry System: phenyl (3-hydroxyphenyl)carbamate(62380-38-5)

Safety Data

• Hazardous Substances Data: 62380-38-5(Hazardous Substances Data)

Usage

General Description

Phenyl (3-hydroxyphenyl)carbamate, also known as TPPO, is an organic compound that contains a phenyl group, a hydroxyphenyl group, and a carbamate functional group. It is commonly used as a reagent in chemical reactions, particularly in the synthesis of pharmaceuticals and agrochemicals. TPPO has been shown to have some antimicrobial and antiviral properties, making it potentially valuable in medical and agricultural applications. Additionally, it has been studied for its potential use as a photoinitiator in the production of advanced materials, such as polymers and composites. Overall, phenyl (3-hydroxyphenyl)carbamate is a versatile chemical with a range of potential uses in various industries.

Upstream product

• 4930-03-4 phenyl N-phenylcarbamate 
• 1885-14-9 phenyl chloroformate 
• 591-27-5 m-Hydroxyaniline 

Downstream Products

• 872167-09-4 7-N-(phenoxycarbonyl)amino-4-chloromethylcoumarin 
• 872167-10-7 7-N-(phenoxycarbonyl)amino-4-(acetylthio)methylcoumarin 
• 279241-53-1 [3-(acridin-9-yl)amino-5-amino]benzyl N-(3-hydroxyphenyl) carbamate 
• 73469-91-7 C₇H₉N₃O₂ 
• 147963-22-2 7-amino-4-(chloromethyl)-2H-1-benzopyran-2-one 

Relevant articles and documents

ISOINDOLINONE COMPOUNDS

Disclosed herein is a compound or pharmaceutically acceptable salts or stereoisomers thereof of of formula I wherein X1 is linear or branched C1-6 alkyl, C3-6 cycloalkyl, -C1-6 alkyl C3-6 cycloalkyl, C6-10 aryl, 5-10 membered heteroaryl, C1-6 alkyl C6-10 aryl, C1-6 alkyl 5-10 membered heteroaryl, wherein X1 is unsubstituted or substituted with one or more of halogen, linear or branched C1-6 alkyl, linear or branched C1-6 heteroalkyl, CF3, CHF2, -O-CHF2, -O-(CH2)2-OMe, OCF3, C1-6 alkylamino, -CN, -N(H)C(O)-C1- 6alkyl, -OC(O)-C1-6alkyl, -OC(O)-C1-4alkylamino, -C(O)O-C1-6alkyl, -COOH, - CHO, -C1-6alkylC(O)OH, -C1-6alkylC(O)O-C1-6alkyl, NH2, C1-6 alkoxy or C1-6 alkylhydroxy; X2 is hydrogen, C6-10 aryl, 5-10 membered heteroaryl, -O-(5-10 membered heteroaryl), 4-8 membered heterocycloalkyl, C1-4 alkyl 4-8 membered heterocycloalkyl, -O-(4-8 membered heterocycloalkyl), -O-C1-4 alkyl-(4-8 membered heterocycloalkyl), -OC(O)-C1-4alkyl-4-8 membered heterocycloalkyl or C6 aryloxy, wherein X2 is unsubstituted or substituted with one or more of linear or branched C1-6 alkyl, NH2, NMe2 or 5-6 membered heterocycloalkyl; n is 0, 1 or 2.

ADDITIVE COMPOSITION FOR CULTURE MEDIUM, ADDITIVE COMPOUND FOR CULTURE MEDIUM, AND METHOD FOR CULTURE OF CELLS OR TISSUE USING SAME

The present invention provides a medium additive composition containing a compound represented by the following formula (I), or a salt thereof: {wherein each symbol is as defined in the DESCRIPTION.}

Preparation of substituted semicarbazides from corresponding amines and hydrazines via phenyl carbamates

A simple synthetic procedure for the conversion of amines and hydrazines into substituted semicarbazides was developed. The initial condensation between the desired amine and phenyl chloroformate into phenyl carbamate is followed by the addition of hydrazine under basic conditions. The reaction is tolerable to a variety of functional groups, with mild conditions and high percent yields.