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Carbonofluoridic acid, 4-(trifluoromethyl)phenyl ester, also known as 4-(trifluoromethyl)phenyl fluoroformate, is an organic compound with the chemical formula C8H5F3O2. It is a colorless liquid that is sensitive to moisture and light, and it has a strong, pungent odor. Carbonofluoridic acid, 4-(trifluoromethyl)phenyl ester is primarily used as a reagent in organic synthesis, particularly in the preparation of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential toxicity, it is essential to handle this chemical with proper safety precautions, including the use of personal protective equipment and controlled environments.

2286-43-3

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2286-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2286-43-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,8 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2286-43:
(6*2)+(5*2)+(4*8)+(3*6)+(2*4)+(1*3)=83
83 % 10 = 3
So 2286-43-3 is a valid CAS Registry Number.

2286-43-3SDS

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 [4-(trifluoromethyl)phenyl] carbonofluoridate

1.2 Other means of identification

Product number -
Other names p-Trifluormethylphenoxy-carbonylfluorid

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:2286-43-3 SDS

2286-43-3Upstream product

2286-43-3Relevant academic research and scientific papers

Rearrangement and radical mediated decarboxylation of trimethylsilyl benzoates using xenon difluoride

Nongkunsarn, Pakawan,Ramsden, Christopher A.

, p. 121 - 122 (2007/10/03)

Treatment of trimethylsilyl benzoates 1 with xenon difluoride in CH2Cl2 or C6F6 results in a novel ester rearrangement and formation of aryl fluoroformates 2: rearrangement is not observed in MeCN solution in wh

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