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N-(3,4-dichlorophenyl)-2-methylpropanamide, commonly known as 2,4-dichlorophenyl-2-methylpropionamide, is a synthetic chemical compound with the molecular formula C10H11Cl2NO. It is a derivative of the amide class, characterized by the presence of a carbonyl group (C=O) bonded to a nitrogen atom. The compound features a 3,4-dichlorophenyl group, which consists of a benzene ring with two chlorine atoms attached at the 3rd and 4th positions, and a 2-methylpropanamide group, which includes an isobutyl chain (2-methylpropane) connected to an amide group. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides. Due to its specific structure, it exhibits certain biological activities and is known for its potential applications in controlling the growth of unwanted plants. However, it is essential to handle N-(3,4-dichlorophenyl)-2-methylpropanamide with care, as it may have potential environmental and health implications.

882-14-4

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882-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 882-14-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,8 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 882-14:
(5*8)+(4*8)+(3*2)+(2*1)+(1*4)=84
84 % 10 = 4
So 882-14-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H11Cl2NO/c1-6(2)10(14)13-7-3-4-8(11)9(12)5-7/h3-6H,1-2H3,(H,13,14)

882-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3,4-dichlorophenyl)-2-methylpropanamide

1.2 Other means of identification

Product number -
Other names Propionanilide,4'-dichloro-2-methyl

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:882-14-4 SDS

882-14-4Downstream Products

882-14-4Relevant academic research and scientific papers

Reductive acylation of nitroarenes to anilides by sodium sulfite in carboxylic acids

Ghaffarzadeh, Mohammad,Akhavan, Pegah

supporting information, p. 1417 - 1419 (2016/09/28)

A facile and efficient reductive acylation of aromatic nitro compounds to corresponding anilides using a sodium sulfite-carboxylic acid system for the first time has been reported. The sodium sulfite reagent provides the colorless reductant in combination with stoichiometric amounts of carboxylic acid and enables the formation of anilides from nitroarenes without any additives in good to excellent yields with high purities and simple work-up. Furthermore, this protocol provides a novel and complementary access to some industrially important chemicals in kilogram scale under mild conditions.

Synergistic herbicidal compositions

-

, (2008/06/13)

Synergistic herbicidal activity is displayed by compositions comprising the following two components: (a) a pyrrolidone of the formula STR1 and (b) an acetanilide of the formula STR2 in which R1 is selected from the group consisting of hydrogen, C1 -C4 alkyl, and chlorine; R2 is selected from the group consisting of hydrogen, C2 -C6 alkoxyalkyl, and C3 -C6 carbalkoxyalkyl; R3 is selected from the group consisting of hydrogen, C1 -C4 alkyl, and chlorine; R4 is selected from the group consisting of hydrogen, C1 -C4 alkyl, and chlorine; and R5 is selected from the group consisting of hydrogen, C1 -C4 alkyl, chlorine, and --NHSO2 CF3, at a weight ratio of (a) to (b) of from about 0.1:1 to about 50:1.

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