6969-90-0

Basic information

• Product Name: N N-DIMETHYLPHENYL CARBAMATE
• Synonyms: N N-DIMETHYLPHENYL CARBAMATE;PHENYL N,N-DIMETHYLCARBAMATE;Dimethyl-carbamic acid phenyl ester, 98%
• CAS NO: 6969-90-0
• Molecular Formula: C₉H₁₁NO₂
• Molecular Weight: 165.19
• Mol File: 6969-90-0.mol
• Article Data: 19

Chemical Properties

• Melting Point: 44-45 °C
• Boiling Point: 234.3 °C at 760 mmHg
• Flash Point: 95.5 °C
• Appearance: /
• Density: 1.095 g/cm³
• Vapor Pressure: 0.0534mmHg at 25°C
• Refractive Index: 1.521
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: -1?+-.0.70(Predicted)
• CAS DataBase Reference: N N-DIMETHYLPHENYL CARBAMATE(CAS DataBase Reference)
• NIST Chemistry Reference: N N-DIMETHYLPHENYL CARBAMATE(6969-90-0)
• EPA Substance Registry System: N N-DIMETHYLPHENYL CARBAMATE(6969-90-0)

Safety Data

• Hazardous Substances Data: 6969-90-0(Hazardous Substances Data)

Usage

General Description

"N N-Dimethylphenyl Carbamate" is an organic chemical compound primarily used as an intermediate in the production of pesticides. It is characterized by its carbamate functional group, which enhances its reactivity. However, it can also pose potential hazards, such as being harmful if swallowed, causing skin irritation, severe eye irritation, and respiratory irritation. It has a molecular formula of C9H12NO2 and a molecular weight of 166.196 g/mol. Always refer to safety data sheets for comprehensive and safe handling information.

InChI:InChI=1/C9H11NO2/c1-10(2)9(11)12-8-6-4-3-5-7-8/h3-7H,1-2H3

Upstream product

• 71-43-2 benzene 
• 687-48-9 ethyl N,N-dimethylcarbamate 
• 108-95-2 phenol 
• 16241-04-6 O-phenyl N,N-dimethylthiocarbamate 
• 139-02-6 sodium phenoxide 
• 68-12-2 N,N-dimethyl-formamide 
• 32115-55-2 N,N-Dimethylcarbamidsaeure-trimethylsilylester 
• 1885-14-9 phenyl chloroformate 
• 124-40-3 dimethyl amine 
• 79-44-7 N,N-Dimethylcarbamoyl chloride 

Downstream Products

• 1778-08-1 2-hydroxy-N,N-dimethylbenzamide 
• 5123-13-7 5,5-dimethyl-2-phenyl-1,3,2-dioxaborinane 
• 74537-09-0 2-benzoylphenyl dimethylcarbamate 
• 1452841-54-1 2,6-dibenzoylphenyl dimethylcarbamate 
• 613-37-6 4-methoxylbiphenyl 
• 1401518-75-9 O-(2-trimethylsilyl)phenyl N,N-dimethylcarbamate 
• 7305-06-8 2-methyl-Ν,Ν-dimethylcarbamoyl phenolate 
• 59577-23-0 N,N-dimethyl-2-(2-hydroxyphenyl)acetamide 
• 20662-88-8 2-phenyloxazole 
• 1826-17-1 4-methyl-2-phenyl-thiazole 
• 1826-24-0 4,5-dimethyl-2-phenyl-1,3-thiazole 
• 29945-53-7 1-methyl-5-phenyl-1H-1,2,4-triazole 
• 1278587-21-5 1-methyl-2-phenyl-5-(4-trifluoromethylphenyl)-1H-imidazole 

Relevant articles and documents

Synthesis and reactions of silylcarbamates with bulky substituents

New silylcarbamates containing bulky substituents were synthesized in order to study their reactivity with nucleophilic agents as lactones and chloroformates.We suggest a mechanism for these reactions.Key words: Silicon

Iron(II)/Persulfate Mediated Newman-Kwart Rearrangement

Herein, we report that iron(II)/ammonium persulfate in aqueous acetonitrile mediates the Newman-Kwart rearrangement of O-aryl carbamothioates. Electron-rich substrates react rapidly under moderate heating to afford the rearranged products in excellent yie

Pd(II) catalyzed ortho C-H iodination of phenylcarbamates at room temperature using cyclic hypervalent iodine reagents

A novel approach to access ortho iodinated phenols using cyclic hypervalent iodine reagents through palladium(II) catalyzed C-H activation has been developed through weak coordination. The reaction showed excellent regioselectivity, reactivity and good functional group tolerance. A unique mechanism was proposed.