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Benzoic acid, 4-fluoro-, 3-nitrophenyl ester is a chemical compound with the molecular formula C14H8FNO5. It is an ester derivative of benzoic acid, where the hydroxyl group (-OH) is replaced by a 3-nitrophenyl group. The presence of a fluorine atom at the 4-position and a nitro group at the 3-position on the benzene ring imparts unique properties to Benzoic acid, 4-fluoro-, 3-nitrophenyl ester. This organic molecule is characterized by its aromatic structure and can be used in various chemical reactions and applications, such as in the synthesis of pharmaceuticals or as a chemical intermediate. Due to its specific functional groups, it may exhibit reactivity with nucleophiles and undergo substitution or elimination reactions.

2710-17-0

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2710-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2710-17-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,1 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2710-17:
(6*2)+(5*7)+(4*1)+(3*0)+(2*1)+(1*7)=60
60 % 10 = 0
So 2710-17-0 is a valid CAS Registry Number.

2710-17-0SDS

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 (3-nitrophenyl) 4-fluorobenzoate

1.2 Other means of identification

Product number -
Other names Benzoic acid,4-fluoro-,3-nitrophenyl 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:2710-17-0 SDS

2710-17-0Downstream Products

2710-17-0Relevant academic research and scientific papers

p-Fluorobenzoyl Chloride for Characterization of Active Hydrogen Functional Groups by Fluorine-19 Nuclear Magnetic Resonance Spectrometry

Spratt, M. P.,Dorn, H. C.

, p. 2038 - 2043 (2007/10/02)

The base-catalyzed reactions of p-fluorobenzoyl chloride provide a convenient method for (19)F NMR analysis of alcohols, phenols, carboxylic acids, amines, and thiols.The (19)F chemical shift and yield data for p-fluorobenzoyl derivatives for nearly 100 compounds are presented.The yield data for these p-fluorobenzoyl derivatives suggest a simple, and in many cases, quantitative method for introducing a fluorine tagging group.The (19)F chemical shifts indicate a wide chemical shift range (ca. 10 ppm) for a large number of compounds.Furthermore, most chemical classes (e.g., phenols, alcohols, etc.) have fairly well resolved chemical shift regions.

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