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18585-06-3

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18585-06-3 Usage

General Description

ETHYL 4-CHLORO-3-TRIFLUOROMETHYLCARBANILATE is a chemical compound that is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is a white crystalline solid with a molecular formula of C10H8ClF3NO2 and a molecular weight of 269.62 g/mol. ETHYL 4-CHLORO-3-TRIFLUOROMETHYLCARBANILATE is known for its strong insecticidal and fungicidal properties, making it a valuable ingredient in the production of pesticides. It is also used in the manufacturing of various pharmaceuticals due to its ability to inhibit the growth of certain bacteria and fungi.ETHYL 4-CHLORO-3-TRIFLUOROMETHYLCARBANILATE is hazardous if ingested or inhaled and should be handled with care in a well-ventilated area and with protective equipment.

Check Digit Verification of cas no

The CAS Registry Mumber 18585-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,8 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18585-06:
(7*1)+(6*8)+(5*5)+(4*8)+(3*5)+(2*0)+(1*6)=133
133 % 10 = 3
So 18585-06-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H9ClF3NO2/c1-2-17-9(16)15-6-3-4-8(11)7(5-6)10(12,13)14/h3-5H,2H2,1H3,(H,15,16)

18585-06-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-[4-chloro-3-(trifluoromethyl)phenyl]carbamate

1.2 Other means of identification

Product number -
Other names Ethyl 4-chloro-3-(trifluoromethyl)phenylcarbamate

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:18585-06-3 SDS

18585-06-3Relevant articles and documents

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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