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2366-82-7

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2366-82-7 Usage

Type of compound

chemical compound, carbamate pesticide

Common uses

insecticide and acaricide in agriculture for controlling pests such as mites, aphids, and other insects

Mechanism of action

disrupts the nervous system of target pests, leading to paralysis and death

Known for

strong and long-lasting effects on a wide range of pests

Potential negative effects

harmful to non-target organisms and the environment, leading to concerns about its continued use and potential for environmental contamination

Regulation

heavily regulated and monitored in many countries to minimize its impact on the environment and non-target species.

Check Digit Verification of cas no

The CAS Registry Mumber 2366-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,6 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2366-82:
(6*2)+(5*3)+(4*6)+(3*6)+(2*8)+(1*2)=87
87 % 10 = 7
So 2366-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H7ClF3NO2/c10-6-2-1-3-7(4-6)14-8(15)16-5-9(11,12)13/h1-4H,5H2,(H,14,15)

2366-82-7SDS

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 2,2,2-trifluoroethyl N-(3-chlorophenyl)carbamate

1.2 Other means of identification

Product number -
Other names 2,2,2-trifluoroethyl 3-chlorophenylcarbamate

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:2366-82-7 SDS

2366-82-7Relevant articles and documents

Facile one-pot synthesis of 4-substituted semicarbazides

Bogolubsky, Andrey V.,Moroz, Yurii S.,Mykhailiuk, Pavel K.,Dmytriv, Yurii V.,Pipko, Sergey E.,Babichenko, Liudmyla N.,Konovets, Anzhelika I.,Tolmachev, Andrey

, p. 1063 - 1069 (2015/02/18)

A diverse library of twenty-five 4-mono- and disubstituted semicarbazides was prepared in a one-pot two-step approach. The method includes formation of a carbamate from bis(2,2,2-trifluoroethyl)carbonate or 2,2,2-trifluoroethylchloroformate and a primary or secondary amine and subsequent interaction of the carbamate with hydrazine to result in a semicarbazide. The approach allowed to obtain 4-substituted semicarbazides on a large scale in good yield and high purity. This journal is

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