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Carbamic acid, 2-methylphenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42349-68-8

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42349-68-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42349-68-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,3,4 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 42349-68:
(7*4)+(6*2)+(5*3)+(4*4)+(3*9)+(2*6)+(1*8)=118
118 % 10 = 8
So 42349-68-8 is a valid CAS Registry Number.

42349-68-8Downstream Products

42349-68-8Relevant academic research and scientific papers

Superparamagnetic Fe3O4 Nanoparticles in a Deep Eutectic Solvent: An Efficient and Recyclable Catalytic System for the Synthesis of Primary Carbamates and Monosubstituted Ureas

Inaloo, Iman Dindarloo,Majnooni, Sahar,Esmaeilpour, Mohsen

, p. 3481 - 3488 (2018/07/29)

Superparamagnetic Fe3O4 nanoparticles were used to synthesize various primary carbamates as well as monosubstituted and N,N-disubstituted ureas. This efficient phosgene-free process used urea as an eco-friendly carbonyl source in the presence of a biocompatible deep eutectic solvent (DES) to provide an inexpensive and attractive route that afforded the products in moderate to excellent yields. The employed DES serves both a catalytic role and as the green reaction medium. The magnetic nanocatalyst and DES can been reused several times without a significant loss of activity.

4-Dodecylbenzenesulfonic acid (DBSA) promoted solvent-free diversity-oriented synthesis of primary carbamates, S-thiocarbamates and ureas

Sardarian, Ali Reza,Inaloo, Iman Dindarloo

, p. 76626 - 76641 (2015/09/22)

A simple and highly efficient solvent-free method for the conversion of alcohols, phenols, thiols and amines to primary carbamates, S-thiocarbamates and ureas in the presence of 4-dodecylbenzenesulfonic acid (DBSA) as a cheap and green Bronsted acid reagent has been described. All products were obtained in good to excellent yields and characterized using FT-IR, 1H- and 13C-NMR, MS and CHNS techniques.

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