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2-Fluoro-4,5-dimethoxybenzoic acid is a chemical compound with the molecular formula C10H11FO4. It is a derivative of benzoic acid, featuring a fluorine atom and two methoxy groups attached to the benzene ring. This white solid at room temperature is soluble in various organic solvents and is valued for its potential biological and pharmacological properties, including anti-inflammatory and anti-cancer activities.

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  • 79474-35-4 Structure
  • Basic information

    1. Product Name: 2-Fluoro-4,5-dimethoxybenzoic acid
    2. Synonyms: 2-Fluoro-4,5-dimethoxybenzoic acid
    3. CAS NO:79474-35-4
    4. Molecular Formula: C9H9FO4
    5. Molecular Weight: 200.1637632
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 79474-35-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 295.9±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.298±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. PKA: 3.42±0.10(Predicted)
    10. CAS DataBase Reference: 2-Fluoro-4,5-dimethoxybenzoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Fluoro-4,5-dimethoxybenzoic acid(79474-35-4)
    12. EPA Substance Registry System: 2-Fluoro-4,5-dimethoxybenzoic acid(79474-35-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 79474-35-4(Hazardous Substances Data)

79474-35-4 Usage

Uses

Used in Pharmaceutical Industry:
2-Fluoro-4,5-dimethoxybenzoic acid is used as a building block for the synthesis of various pharmaceuticals due to its unique chemical structure and properties. Its presence in the molecular composition of drugs can contribute to their therapeutic effects, particularly in the treatment of inflammation and cancer.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Fluoro-4,5-dimethoxybenzoic acid is utilized as a precursor in the development of agrochemicals. Its chemical properties make it suitable for the creation of compounds that can be used in pest control and crop protection, enhancing agricultural productivity and crop quality.
Used in Organic Synthesis:
2-Fluoro-4,5-dimethoxybenzoic acid is employed as an intermediate in organic synthesis for the preparation of a wide range of chemical compounds. Its versatility in chemical reactions allows for the production of various specialty chemicals used across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 79474-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,7 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79474-35:
(7*7)+(6*9)+(5*4)+(4*7)+(3*4)+(2*3)+(1*5)=174
174 % 10 = 4
So 79474-35-4 is a valid CAS Registry Number.

79474-35-4SDS

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 2-Fluoro-4,5-dimethoxybenzoic acid

1.2 Other means of identification

Product number -
Other names 6-fluoroveratric acid

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:79474-35-4 SDS

79474-35-4Relevant articles and documents

PYRROLOPYRAZINE-SPIROCYCLIC PIPERIDINE AMIDES AS MODULATORS OF ION CHANNELS

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Paragraph 0363; 0364, (2013/03/26)

The invention relates to pyrrolopyrazine-spirocyclic piperidine amide compounds useful as inhibitors of ion channels. The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various disorders.

Synthesis of fluoro- and polyfluoro-veratraldehydes by electrophilic fluorination

Nie, Jun-ying,Kirk, Kenneth L.

, p. 297 - 302 (2007/10/03)

Lithiation of oxazolines derived from fluorinated veratric acid, followed by electrophilic fluorination and subsequent reductive oxazoline cleavage, provides a convenient route to di- and tri-fluoroveratraldehydes.Similarly, 4-fluoroveratrol was converted

Synthesis and EPR Investigations of Fluorocatecholamines

Stegmann, Hartmut B.,Deuschle, Gabriele,Schuler, Paul

, p. 547 - 556 (2007/10/02)

The synthesis of 3-fluoro and 5-fluoronoradrenaline (3- and 5-fluoronorepinephrine) starting from 4-fluorophenol or 3-fluoroanisole is described.In the first step the second OH group is introduced followed by O-methylation and subsequent introduction of a

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