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2,4,6-trimethylphenyl methylcarbamate is a chemical compound with the molecular formula C11H15NO2. It is an organic compound that belongs to the class of carbamates, which are derivatives of carbamic acid. This specific compound features a trimethylphenyl group, which consists of a benzene ring with three methyl groups attached at the 2, 4, and 6 positions, and a methylcarbamate group, which is a carbamate functional group with a methyl group attached. 2,4,6-trimethylphenyl methylcarbamate is known for its potential use as an insecticide, although it is not widely used in modern agriculture due to the availability of more effective and safer alternatives. The compound is also of interest in chemical research for its unique structure and potential applications in the synthesis of other organic compounds.

3971-92-4

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3971-92-4 Usage

Chemical class

Carbamate pesticides.

Primary use

Insecticide and acaricide.

Mode of action

Inhibits the activity of the enzyme acetylcholinesterase in insects and mites.

Effect on pests

Disrupts the nervous system of pests, ultimately causing their death.

Target pests

Aphids, mites, leafhoppers, and whiteflies.

Applicable crops

Cotton, vegetables, and fruit orchards.

Toxic properties

Poses risks to human health and the environment.

Precaution

Handle and use trimethacarb with care.

Check Digit Verification of cas no

The CAS Registry Mumber 3971-92-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,7 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3971-92:
(6*3)+(5*9)+(4*7)+(3*1)+(2*9)+(1*2)=114
114 % 10 = 4
So 3971-92-4 is a valid CAS Registry Number.

3971-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,4,6-trimethylphenyl) N-methylcarbamate

1.2 Other means of identification

Product number -
Other names Mesityl methylcarbamate

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:3971-92-4 SDS

3971-92-4Downstream Products

3971-92-4Relevant academic research and scientific papers

A method of synthesizing aromatic carbamate

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Paragraph 0106-0107, (2018/02/04)

The invention relates to a synthetic method for romatic carbamic acid ester. The method comprises the following steps: adding diaryliodonium salt, amine, alkali and an organic solvent into a high-pressure reaction kettle, wherein diaryliodonium salt and a

Base-Promoted Coupling of Carbon Dioxide, Amines, and Diaryliodonium Salts: A Phosgene- and Metal-Free Route to O-Aryl Carbamates

Xiong, Wenfang,Qi, Chaorong,Peng, Youbin,Guo, Tianzuo,Zhang, Min,Jiang, Huanfeng

supporting information, p. 14314 - 14318 (2015/10/05)

A phosgene- and metal-free synthesis of O-aryl carbamates is realized through a three-component coupling of carbon dioxide, amines and diaryliodonium salts. The reaction only requires a base as the promoter, providing access to a diverse array of O-aryl c

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