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methyl (2,3-dimethylphenyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20642-94-8

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20642-94-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20642-94-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,4 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20642-94:
(7*2)+(6*0)+(5*6)+(4*4)+(3*2)+(2*9)+(1*4)=88
88 % 10 = 8
So 20642-94-8 is a valid CAS Registry Number.

20642-94-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl N-(2,3-dimethylphenyl)carbamate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:20642-94-8 SDS

20642-94-8Downstream Products

20642-94-8Relevant academic research and scientific papers

Synthesis of aryl urea derivatives from aryl amines and aryl isocyanates

Usharani,Bhujanga Rao,Reddy,Dubey

, p. 1802 - 1806 (2011/12/22)

The present study describes the synthesis of novel diaryl urea derivatives derived from aryl amine and aryl isocyanates. The synthesized compounds are analogs of sorafenib [4-[4-[[[4-chloro-3-(trifluoromethyl)phenyl]amino]carbonyl] amino]phenoxy]-N-methylpyridine-2- carboxamide] having potential antiproliferative activity.

Selective N,N-dimethylation of primary aromatic amines with methyl alkyl carbonates in the presence of phosphonium salts

Selva, Maurizio,Perosa, Alvise,Tundo, Pietro,Brunelli, Davide

, p. 5770 - 5773 (2007/10/03)

In the presence of onium salts, at 140-170 °C. methyl alkyl carbonates [1a-c, ROCO2Me, R = MeO(CH2)2[O(CH 2)2]n; n = 2-0, respectively] react with primary aromatic amines (XC6H4NH2, X = p-OMe, p-Me, H, p-Cl, p-CO2Me, o-Et, and 2,3-Me2C 6H3NH2) to yield the corresponding N,N-dimethyl derivatives (ArNMe2) with high selectivity (up to 96%) and good isolated yields (78-95%). Phosphonium salts (e.g., Ph3PEtI and n-Bu4PBr) are particularly efficient catalysts. Overall, a solvent-free reaction is coupled with safe methylating agents (1a-c) made from nontoxic dimethyl carbonate.

Indirect electrochemical carbonylation of aromatic amines with a palladium catalyst

Hartstock, Frederick W.,Herrington, Deborah G.,McMahon, Launa B.

, p. 8761 - 8764 (2007/10/02)

Aromatic amines are converted to carbamates under very mild conditions, using carbon monoxide, palladium (II) acetate and copper (II) acetate in combination with anodic reoxidation.

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