6324-13-6

Basic information

• Product Name: N-[2-(Ethoxycarbonylamino)phenyl]carbamic acid ethyl ester
• Synonyms: 1,2-Phenylenebis(carbamic acid ethyl) ester;N-[2-(Ethoxycarbonylamino)phenyl]carbamic acid ethyl ester;di-tert-butyl 1,3-phenylenedicarbamate
• CAS NO: 6324-13-6
• Molecular Formula: C₁₂H₁₆N₂O₄
• Molecular Weight: 252.27
• Mol File: 6324-13-6.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 292.4°C at 760 mmHg
• Flash Point: 130.6°C
• Appearance: /
• Density: 1.252g/cm³
• Vapor Pressure: 0.00184mmHg at 25°C
• Refractive Index: 1.585
• CAS DataBase Reference: N-[2-(Ethoxycarbonylamino)phenyl]carbamic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-(Ethoxycarbonylamino)phenyl]carbamic acid ethyl ester(6324-13-6)
• EPA Substance Registry System: N-[2-(Ethoxycarbonylamino)phenyl]carbamic acid ethyl ester(6324-13-6)

Safety Data

• Hazardous Substances Data: 6324-13-6(Hazardous Substances Data)

Usage

General Description

N-[2-(Ethoxycarbonylamino)phenyl]carbamic acid ethyl ester is a chemical compound that consists of a carbamic acid ethyl ester attached to a phenyl group with an ethoxycarbonylamino functional group. It is commonly used in organic synthesis and as a reagent in chemical reactions. N-[2-(Ethoxycarbonylamino)phenyl]carbamic acid ethyl ester is also an important intermediate in the production of pharmaceuticals and agrochemicals. It has the potential to be toxic if inhaled or swallowed, and it can cause irritation to the skin and eyes upon contact. Overall, N-[2-(Ethoxycarbonylamino)phenyl]carbamic acid ethyl ester is a versatile compound with various applications in the field of chemistry.

InChI:InChI=1/C12H16N2O4/c1-3-17-11(15)13-9-7-5-6-8-10(9)14-12(16)18-4-2/h5-8H,3-4H2,1-2H3,(H,13,15)(H,14,16)

Upstream product

• 64-17-5 ethanol 
• 65325-59-9 N-azidocarbonyl-anthraniloyl azide 
• 95-54-5 1,2-diamino-benzene 
• 541-41-3 chloroformic acid ethyl ester 
• 88-74-4 2-nitro-aniline 
• 129922-60-7 ethyl 2-(2-aminoanilino)cycloheptapyrrole-3-carboxylate 

Downstream Products

• 3213-79-4 N,N'-dimethyl-1,2-phenylenediamine 
• 53439-88-6 5-amino-1,3-dimethyl-1,3-dihydro-2H-benzo[d]imidazol-2-one 
• 615-16-7 1,3-dihydro-2H-benzimidazol-2-one 
• 15719-64-9 methylammonium carbonate 

Relevant articles and documents

Palladium-Catalyzed Modular Synthesis of Substituted Piperazines and Related Nitrogen Heterocycles

We report here a novel method for the modular synthesis of highly substituted piperazines and related bis-nitrogen heterocycles via a palladium-catalyzed cyclization reaction. The process couples two of the carbons of a propargyl unit with various diamine components to provide nitrogen heterocycles in generally good to excellent yields and high regio- and stereochemical control. (Chemical Equation Presented).

Titanium and zirconium complexes of robust salophan ligands. Coordination chemistry and olefin polymerization catalysis

The synthesis of [ONNO]-type robust Salophan ligands featuring tertiary nitrogen donors is described for the first time. By varying the substitution pattern on the aromatic bridge and on the phenolate rings, four ligands possessing a broad scope of electr

Microwave promoted solvent-free one-pot synthesis of N,N′- disubstituted urea derivatives

An efficient one-pot synthesis of N,N′-disubstituted urea derivatives from substituted anilines, ethyl chloroformate and methyl anthranilate or methyl 3-amino-2-butenoate under microwave irradiation is reported.