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METHYL (3,5-DICHLOROPHENYL)CARBAMATE, commonly known as a carbamate pesticide and insecticide, is a chemical compound that functions by inhibiting the activity of acetylcholinesterase enzyme in insects. This inhibition leads to the accumulation of acetylcholine in the nervous system, causing paralysis and death in pests. It is effective against a broad spectrum of agricultural pests and is utilized for the protection of various crops.

25217-43-0

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25217-43-0 Usage

Uses

Used in Agricultural Industry:
METHYL (3,5-DICHLOROPHENYL)CARBAMATE is used as a pesticide for the control of a wide range of agricultural pests. It is applied to protect various crops by targeting and eliminating insects that can cause significant damage to the plants, thereby ensuring crop yield and quality.
Used in Insecticide Formulations:
METHYL (3,5-DICHLOROPHENYL)CARBAMATE is used as an active ingredient in insecticide formulations to combat insect infestations in both agricultural and non-agricultural settings. Its effectiveness in disrupting the nervous system of insects makes it a valuable tool in controlling and preventing infestations that can cause harm to plants, animals, and humans.

Check Digit Verification of cas no

The CAS Registry Mumber 25217-43-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,1 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25217-43:
(7*2)+(6*5)+(5*2)+(4*1)+(3*7)+(2*4)+(1*3)=90
90 % 10 = 0
So 25217-43-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H7Cl2NO2/c1-13-8(12)11-7-3-5(9)2-6(10)4-7/h2-4H,1H3,(H,11,12)

25217-43-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl N-(3,5-dichlorophenyl)carbamate

1.2 Other means of identification

Product number -
Other names 3,5-Dichlorocarbanilic acid methyl ester

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:25217-43-0 SDS

25217-43-0Downstream Products

25217-43-0Relevant academic research and scientific papers

Electrochemical Hofmann rearrangement mediated by NaBr: Practical access to bioactive carbamates

Li, Lijun,Xue, Mengyu,Yan, Xin,Liu, Wenmin,Xu, Kun,Zhang, Sheng

supporting information, p. 4615 - 4618 (2018/07/06)

An electrochemical Hofmann rearrangement is reported. With the mediation of NaBr, highly corrosive and toxic halogens are avoided. Moreover, this efficient and green approach is well compatible with a broad range of amides, including several commercial medicine derivatives, and provides direct access to synthetically useful carbamates. The synthetic utility of this method is also demonstrated by the preparation of 15N labeling carbamate and gram-scale synthesis of Amantadine.

Photochemistry of vinclozolin in water and methanol-water solution

Schick,Moza,Hustert,Kettrup

, p. 1116 - 1122 (2007/10/03)

The photolysis of the fungicide vinclozolin in aqueous and methanol- water (50+50 by volume) solution has been examined. Irradiation at λ=254nm for 10 minutes resulted in 2 moiety takes place, and one or both the chlorine atoms are replaced by a methoxy group.

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