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5043-00-5

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5043-00-5 Usage

Description

6-FLUORO-2-NAPHTHOIC ACID METHYL ESTER is a chemical compound characterized by the molecular formula C13H9FO2. It is a derivative of naphthoic acid, featuring a fluorine atom at the 6-position and a methyl ester group. This fluorinated compound is recognized for its potential biological activities and is widely utilized as a building block in the synthesis of pharmaceuticals and agrochemicals. Its stability and ease of handling in laboratory settings are enhanced by its methyl ester form.

Uses

Used in Pharmaceutical Industry:
6-FLUORO-2-NAPHTHOIC ACID METHYL ESTER is used as a key intermediate in the synthesis of various pharmaceuticals for its potential biological activities. It contributes to the development of new drugs by providing a structural foundation that can be further modified to achieve desired therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, 6-FLUORO-2-NAPHTHOIC ACID METHYL ESTER is employed as a precursor in the production of agrochemicals. Its unique chemical properties allow for the creation of compounds with specific pesticidal or herbicidal activities, enhancing crop protection and yield.
Used in Organic Synthesis:
6-FLUORO-2-NAPHTHOIC ACID METHYL ESTER is utilized as a reagent in organic synthesis, facilitating the formation of complex organic molecules. Its presence can influence the reactivity and selectivity of reactions, enabling the synthesis of a wide range of organic compounds.
Used in Production of Fluorine-Containing Compounds:
As a starting material, 6-FLUORO-2-NAPHTHOIC ACID METHYL ESTER is essential in the production of other fluorine-containing compounds. The introduction of fluorine atoms into organic molecules can significantly alter their properties, making this compound a valuable resource in the synthesis of fluorinated materials with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5043-00-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,4 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5043-00:
(6*5)+(5*0)+(4*4)+(3*3)+(2*0)+(1*0)=55
55 % 10 = 5
So 5043-00-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H9FO2/c1-15-12(14)10-3-2-9-7-11(13)5-4-8(9)6-10/h2-7H,1H3

5043-00-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 6-Fluoro-2-naphthoate

1.2 Other means of identification

Product number -
Other names 6-Fluoro-2-naphthoic Acid Methyl 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:5043-00-5 SDS

5043-00-5Relevant articles and documents

De Novo Synthesis of Phenols and Naphthols through Oxidative Cycloaromatization of Dienynes

Rong, Ming-Guang,Qin, Tian-Zhu,Liu, Xin-Rui,Wang, Hong-Fa,Zi, Weiwei

supporting information, p. 6289 - 6293 (2018/10/09)

In this work, a rhodium-catalyzed oxidative cycloaromatization of dienynes, which provides a highly straightforward and efficient way to access polysubstituted naphthols and phenols under mild conditions, is described. Challenged electron-withdrawing groups are well tolerated in this protocol, and late-stage phenyl ring formation is demonstrated.

Palladium-Catalyzed Alkynylation of Morita-Baylis-Hillman Carbonates with (Triisopropylsilyl)acetylene on Water

Li, Yangxiong,Liu, Li,Kong, Delong,Wang, Dong,Feng, Weichun,Yue, Tao,Li, Chaojun

, p. 6283 - 6290 (2015/06/30)

Direct alkynylation of Morita-Baylis-Hillman carbonates with (triisopropylsilyl)acetylene catalyzed by a Pd(OAc)2-NHC complex was developed "on water" to give the corresponding 1,4-enynes. The significant effects of water amount in the solvent

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