7244-70-4

Basic information

• Product Name: 4-nitrophenyl dimethylcarbamate
• Synonyms: 4-nitrophenyl dimethylcarbamate
• CAS NO: 7244-70-4
• Molecular Formula: C₉H₁₀N₂O₄
• Molecular Weight: 210.1867
• Mol File: 7244-70-4.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 329.1°Cat760mmHg
• Flash Point: 152.9°C
• Appearance: /
• Density: 1.292g/cm³
• Vapor Pressure: 0.000181mmHg at 25°C
• Refractive Index: 1.558
• CAS DataBase Reference: 4-nitrophenyl dimethylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-nitrophenyl dimethylcarbamate(7244-70-4)
• EPA Substance Registry System: 4-nitrophenyl dimethylcarbamate(7244-70-4)

Safety Data

• Hazardous Substances Data: 7244-70-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H10N2O4/c1-10(2)9(12)15-8-5-3-7(4-6-8)11(13)14/h3-6H,1-2H3

Upstream product

• 5070-13-3 bis-(p-nitrophenyl) carbonate 
• 124-40-3 dimethyl amine 
• 100-02-7 4-nitro-phenol 
• 79-44-7 N,N-Dimethylcarbamoyl chloride 

Downstream Products

• 14609-74-6 p-nitrophenolate 
• 7260-94-8 N,N-dimethylcarbamic acid 
• 16088-19-0 norneostigmine 
• 1631050-39-9 C₉H₁₀N₂O₅ 
• 3316-09-4 1,2-dihydroxy-4-nitrobenzene 
• 19962-04-0 Dimethylcarbaminsaeure-3-aminophenylester 
• 1380586-35-5 2-bromo-4-nitrophenyl dimethylcarbamate 
• 25272-70-2 O-Dimethylcarbamoyl-acetamidoxim 

Relevant articles and documents

HIGHLY CHEMOSELECTIVE REACTIONS IN PRESENCE OF AROMATIC AMINO GROUPS

: The invention discloses a novel process for highly chemoselective reactions of substituted anilines without any detectable reaction at aromatic amino group. The invention also relates to a novel process for preparation of neostigmine methylsulphate via chemoselective reaction of 3-amionphenol and aryl dimethylcarbamates.

A general approach towards catechol and pyrogallol through ruthenium- and palladium-catalyzed C-H hydroxylation by weak coordination

An efficient ruthenium(II)- and palladium(II)-catalyzed C-H hydroxylation of aryl carbamates has been developed for the facile synthesis of catechols and pyrogallols. The reaction demonstrates excellent reactivity, regio- and chemoselectivity, good functional group compatibility and high yields. The practicality of this method has been proved by a gram-scale synthesis.

PROCESS FOR PREPARATION OF HIGHLY PURE 3-DIMETHYLAMINOPHENYL DIMETHYLCARBAMATE

The invention discloses a novel process for preparation of highly pure 3-dimethylaminophenyl dimethylcarbamate via formation of aryl dimethylcarbamate which can be easily obtained from diaryl carbonate and dimethylamine.