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Ethyl (3-fluorophenyl)carbamate is an organic compound with the chemical formula C9H10FNO2. It is a derivative of phenylcarbamic acid, where one of the hydrogen atoms on the phenyl ring is replaced by a fluorine atom, and the carbamic acid group is esterified with ethanol. ethyl (3-fluorophenyl)carbamate is characterized by its potential applications in pharmaceuticals and agrochemicals, particularly as a precursor in the synthesis of various drugs and pesticides. It is important to note that due to its reactivity and potential toxicity, ethyl (3-fluorophenyl)carbamate should be handled with care, following appropriate safety protocols.

403-92-9

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403-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 403-92-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 403-92:
(5*4)+(4*0)+(3*3)+(2*9)+(1*2)=49
49 % 10 = 9
So 403-92-9 is a valid CAS Registry Number.

403-92-9SDS

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 m-fluorophenyl carbamate

1.2 Other means of identification

Product number -
Other names N-<3-Fluor-phenyl>(3-fluoro-phenyl)-carbamic acid ethyl 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:403-92-9 SDS

403-92-9Relevant academic research and scientific papers

Synthesis and antibacterial activity of isothiazolyl oxazolidinones and analogous 3(2H)-isothiazolones

Adibpour, Neda,Khalaj, Ali,Rajabalian, Saeed

scheme or table, p. 19 - 24 (2010/03/24)

The synthesis and antibacterial activity of several new 5-((3-oxoisothiazol-2(3H)-yl)methyl)-3-phenyloxazolidin-2-ones 8 and analogous 2-(4-substituted phenyl)-3(2H)-isothiazolones 3 and 4 substituted at 4 and/or 3-positions of the phenyl moiety with different groups of which some have shown to increase the antibacterial activity of both 3-aryl-2-oxazolidinones and 3(2H)-isothiazolones is described. The most active compounds were isothiazolyl oxazolidinones 8a,j with unsubstituted and 8b with 4-F substituted phenyl rings which showed activities higher than analogous 3(2H)-isothiazolones and comparable or superior to linezolid, vancomycin, and ciprofloxacin against some tested microorganisms. The change in position of F and/or the use of larger substituents gave compounds with reduced or no activity. Evaluation of cytotoxicity to mouse fibroblast (NIH/3T3) cells indicated that these compounds exhibit antibacterial activity at non-cytotoxic concentrations.

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