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2,4-dichloro-N,N-dimethylbenzamide, commonly known as dimethachlor, is a chloroacetanilide herbicide with the molecular formula C9H10Cl2N2O. It is a white crystalline solid with a slightly sweet odor and is soluble in organic solvents but not in water. This chemical compound is used to control broadleaf weeds and grasses in various crops by inhibiting the synthesis of fatty acids in plants, ultimately leading to their death. Dimethachlor is considered to have low toxicity to mammals and aquatic organisms, but it is important to handle and use it with caution, following all safety guidelines and regulations.

6333-36-4

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6333-36-4 Usage

Uses

Used in Agricultural Industry:
2,4-dichloro-N,N-dimethylbenzamide is used as a herbicide for controlling broadleaf weeds and grasses in various crops. It is effective in inhibiting the synthesis of fatty acids in plants, which leads to their death, thus protecting the crops from unwanted plant growth.
Used in Weed Management:
2,4-dichloro-N,N-dimethylbenzamide is used as a weed management tool to ensure the healthy growth of crops by eliminating unwanted plant species that compete for resources and may cause damage to the cultivated plants. Its selective action on weeds makes it a valuable component in integrated pest management strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 6333-36-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6333-36:
(6*6)+(5*3)+(4*3)+(3*3)+(2*3)+(1*6)=84
84 % 10 = 4
So 6333-36-4 is a valid CAS Registry Number.

6333-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Dichlor-m-phenylendiisocyanat

1.2 Other means of identification

Product number -
Other names 2,4-Dichlor-N,N-dimethylbenzamid

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:6333-36-4 SDS

6333-36-4Relevant academic research and scientific papers

Anion conductive aromatic copolymers from dimethylaminomethylated monomers: Synthesis, properties, and applications in alkaline fuel cells

Akiyama, Ryo,Yokota, Naoki,Nishino, Eriko,Asazawa, Koichiro,Miyatake, Kenji

, p. 4480 - 4489 (2016/07/07)

A novel series of anion conductive aromatic copolymers were synthesized from preaminated monomers (2,5-, 3,5-, or 2,4-dichloro-N,N-dimethylbenzylamine), and their properties were investigated for alkaline fuel cell applications. The targeted copolymers (QPE-bl-11a, -11b, and -11c) were synthesized via nickel-mediated Ullmann coupling polymerization, followed by quaternization and ion exchange reactions. Unlike the conventional method involving chloromethylation or bromination, this method provided copolymers with well-defined chemical structure. The hydrophilic components of the copolymers were composed of chemically stable phenylene main chain modified with high-density ammonium groups. Oligo(arylene ether sulfone ketone)s were employed as a hydrophobic block. QPE-bl-11a gave tough and bendable membranes by solution casting. The obtained membrane with the highest ion exchange capacity value (IEC = 2.47 mequiv g-1) showed high hydroxide ion conductivity (130 mS cm-1) in water at 80 °C. The QPE-bl-11a membrane showed reasonable alkaline stability in 1 M KOH aqueous solution for 1000 h at 60 °C. A platinum-free fuel cell was successfully operated with hydrazine as a fuel, the QPE-bl-11a as a membrane, and an electrode binder. The maximum power density of 380 mW cm-2 was achieved at a current density of 1020 mA cm-2 with O2.

Process for preparing 5-aroyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylates (II) and intermediates therefor

-

, (2008/06/13)

5-Aroyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylates of the formula STR1 are prepared from 2-aroylpyrroles. Hydrolysis and mono-decarboxylation of these compounds affords ketorolac and related compounds.

Process for preparing 5-aroyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylates (I) and intermediates therefor

-

, (2008/06/13)

5-Aroyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylates of the formula STR1 are prepared from 2-aroylpyrroles. Hydrolysis and mono-decarboxylation of these compounds affords ketorolac and related compounds.

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