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25217-43-0

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25217-43-0 Usage

General Description

Methyl (3,5-dichlorophenyl)carbamate is a chemical compound that is commonly used as a pesticide and insecticide. It is a type of carbamate, which means it works by inhibiting the activity of an enzyme called acetylcholinesterase, leading to the accumulation of acetylcholine in the nervous system of insects, ultimately resulting in their paralysis and death. This chemical is effective against a wide range of agricultural pests and is used in the protection of various crops. However, methyl (3,5-dichlorophenyl)carbamate is also toxic to humans and can cause adverse health effects if not handled and used properly. Therefore, it is important to follow safety guidelines and regulations when using this chemical.

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 articles and documents

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.

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