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Ethyl (3-chloro-2-fluorophenyl)carbamate is a chemical compound with the molecular formula C9H8ClFNO2. It is an organofluorine compound, which means it contains a carbon-fluorine bond, and is a derivative of phenylcarbamic acid. ethyl (3-chloro-2-fluorophenyl)carbamate is characterized by a chlorofluorophenyl group attached to an ethyl carbamate moiety. It is synthesized through the reaction of 3-chloro-2-fluorophenol with ethyl isocyanate. Ethyl (3-chloro-2-fluorophenyl)carbamate is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. Due to its potential applications in these areas, it is important to understand its chemical properties and reactivity.

2317-75-1

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2317-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2317-75-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,1 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2317-75:
(6*2)+(5*3)+(4*1)+(3*7)+(2*7)+(1*5)=71
71 % 10 = 1
So 2317-75-1 is a valid CAS Registry Number.

2317-75-1SDS

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 ethyl N-(3-chloro-2-fluorophenyl)carbamate

1.2 Other means of identification

Product number -
Other names -

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:2317-75-1 SDS

2317-75-1Downstream Products

2317-75-1Relevant academic research and scientific papers

Teaching Old Compounds New Tricks: DDQ-Photocatalyzed C?H Amination of Arenes with Carbamates, Urea, and N-Heterocycles

Das, Somnath,Natarajan, Palani,K?nig, Burkhard

supporting information, p. 18161 - 18165 (2017/12/28)

The C?H amination of benzene derivatives was achieved using DDQ as photocatalyst and BocNH2 as the amine source under aerobic conditions and visible light irradiation. Electron-deficient and electron-rich benzenes react as substrates with moderate to good product yields. The amine scope of the reaction comprises Boc-amine, carbamates, pyrazoles, sulfonimides and urea. Preliminary mechanistic investigations indicate arene oxidation by the triplet of DDQ to radical cations with different electrophilicity and a charge transfer complex between the amine and DDQ as intermediate of the reaction.

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