2610-61-9

Basic information

• Product Name: (3-HYDROXY-PHENYL)-CARBAMIC ACID ISOPROPYL ESTER
• Synonyms: ISOPROPYL (3-HYDROXYPHENYL)CARBAMATE;(3-HYDROXY-PHENYL)-CARBAMIC ACID ISOPROPYL ESTER
• CAS NO: 2610-61-9
• Molecular Formula: C₁₀H₁₃NO₃
• Molecular Weight: 195.22
• Mol File: 2610-61-9.mol
• Article Data: 2

Chemical Properties

• Melting Point: 78-80 °C
• Boiling Point: 276.3±23.0 °C(Predicted)
• Appearance: /
• Density: 1.214±0.06 g/cm3(Predicted)
• PKA: 9.80±0.10(Predicted)
• CAS DataBase Reference: (3-HYDROXY-PHENYL)-CARBAMIC ACID ISOPROPYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: (3-HYDROXY-PHENYL)-CARBAMIC ACID ISOPROPYL ESTER(2610-61-9)
• EPA Substance Registry System: (3-HYDROXY-PHENYL)-CARBAMIC ACID ISOPROPYL ESTER(2610-61-9)

Safety Data

• Hazardous Substances Data: 2610-61-9(Hazardous Substances Data)

Usage

General Description

The chemical (3-Hydroxy-phenyl)-carbamic acid isopropyl ester, also known as isopropyl 3-hydroxyphenylcarbamate, is an organic compound with the molecular formula C11H13NO3. It is a derivative of phenylcarbamic acid and isopropyl alcohol. (3-HYDROXY-PHENYL)-CARBAMIC ACID ISOPROPYL ESTER is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has potential applications in the field of medicine and agriculture due to its ability to inhibit enzymes and act as a biological active agent. However, it is important to handle and use this compound with caution, as it can be hazardous if not properly managed. Overall, isopropyl 3-hydroxyphenylcarbamate has potential uses in various industries and research fields due to its chemical properties and potential biological activities.

Upstream product

• 108-23-6 isopropyl chloroformate 
• 591-27-5 m-Hydroxyaniline 
• 101-21-3 CHLORPROPHAM 

Downstream Products

• 23122-11-4 C₁₇H₁₇FN₂O₄ 
• 23122-12-5 C₁₈H₂₀N₂O₄ 
• 23122-39-6 (3-Bromo-4-fluoro-phenyl)-carbamic acid 3-isopropoxycarbonylamino-phenyl ester 

Relevant articles and documents

Ultrasonic and photochemical degradation of chlorpropham and 3-chloroaniline in aqueous solution

Sonolysis and photolysis are compared for the transformation of chlorpropham, a systemic herbicide belonging to the carbamate group, and 3-chloroaniline, the main intermediate often observed in the degradation of chlorpropham. In both cases the ultrasonic degradation is much more efficient at 482 kHz than at 20 kHz. The main identified sonoproducts formed in the degradation of chlorpropham are 3-chloroaniline, formic acid, carbon monoxide and dioxide and chloride ions. The degradation of 3-chloroaniline also leads to Cl-, CO and CO2 but chlorohydroquine was also detected as an intermediate. Two different mechanisms are involved in the ultrasonic transformation: pyrolysis resulting from the implosion of cavitation microbubbles and oxidation by hydroxyl radicals formed by sonolysis of water. Photolysis is more specific: 3-chloroaniline is initially quantitatively transformed into 3-aminophenol. A heterolytic mechanism is suggested. Resorcinol and some unidentified photoproducts are formed in a second stage. The same type of reaction is involved in the photo-transformation of chlorpropham, but the reaction is not so specific. In both cases the photolysis at 254 nm leads to a complete disappearance of phenolic and quinonic compounds. Sonolysis and photolysis are compared for the transformation of chlorpropham, a systemic herbicide belonging to the carbamate group, and 3-chloroaniline, the main intermediate often observed in the degradation of chlorpropham. In both cases the ultrasonic degradation is much more efficient at 482 kHz than at 20 kHz. The main identified sonoproducts formed in the degradation of chlorpropham are 3-chloroaniline, formic acid, carbon monoxide and dioxide and chloride ions. The degradation of 3-chloroaniline also leads to Cl-, CO and CO2 but chlorohydroquine was also detected as an intermediate. Two different mechanisms are involved in the ultrasonic transformation: pyrolysis resulting from the implosion of cavitation microbubbles and oxidation by hydroxyl radicals formed by sonolysis of water. Photolysis is more specific: 3-chloroaniline is initially quantitatively transformed into 3-amino-phenol. A heterolytic mechanism is suggested. Resorcinol and some unidentified photoproducts are formed in a second stage. The same type of reaction is involved in the photo-transformation of chlorpropham, but the reaction is not so specific. In both cases the photolysis at 254 nm leads to a complete disappearance of phenolic and quinonic compounds.