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1113049-61-8

2-AMino-4-fluoro-5-hydroxy-benzoic acid Methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1113049-61-8 Structure

  • Basic information

    1. Product Name: 2-AMino-4-fluoro-5-hydroxy-benzoic acid Methyl ester
    2. Synonyms: 2-AMino-4-fluoro-5-hydroxy-benzoic acid Methyl ester;methyl 2-amino-4-fluoro-5-hydroxybenzoate
    3. CAS NO:1113049-61-8
    4. Molecular Formula: C8H8FNO3
    5. Molecular Weight: 185.1524232
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1113049-61-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 344.1±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.400±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 8.17±0.23(Predicted)
    10. CAS DataBase Reference: 2-AMino-4-fluoro-5-hydroxy-benzoic acid Methyl ester(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-AMino-4-fluoro-5-hydroxy-benzoic acid Methyl ester(1113049-61-8)
    12. EPA Substance Registry System: 2-AMino-4-fluoro-5-hydroxy-benzoic acid Methyl ester(1113049-61-8)

  • 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: 1113049-61-8(Hazardous Substances Data)

1113049-61-8 Usage

General Description

2-Amino-4-fluoro-5-hydroxy-benzoic acid methyl ester is a chemical compound that belongs to the class of benzoic acids. It is a derivative of salicylic acid and is commonly used in the pharmaceutical industry as an intermediate in the synthesis of various drugs. 2-AMino-4-fluoro-5-hydroxy-benzoic acid Methyl ester is known for its potential biological activities, including anti-inflammatory and analgesic properties. Additionally, it has been studied for its potential use in the treatment of neurodegenerative diseases. Its methyl ester form makes it more stable and easier to handle, and it is often used in organic synthesis as a reagent for the preparation of other compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1113049-61-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,3,0,4 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1113049-61:
(9*1)+(8*1)+(7*1)+(6*3)+(5*0)+(4*4)+(3*9)+(2*6)+(1*1)=98
98 % 10 = 8
So 1113049-61-8 is a valid CAS Registry Number.

1113049-61-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2-amino-4-fluoro-5-hydroxybenzoate

1.2 Other means of identification

Product number -
Other names 2-Amino-4-fluoro-5-hydroxybenzoic 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:1113049-61-8 SDS

1113049-61-8Relevant articles and documents

Structure-based design of novel HCV NS5B thumb pocket 2 allosteric inhibitors with submicromolar gt1 replicon potency: Discovery of a quinazolinone chemotype

Beaulieu, Pierre L.,Coulombe, René,Duan, Jianmin,Fazal, Gulrez,Godbout, Cédrickx,Hucke, Oliver,Jakalian, Araz,Joly, Marc-André,Lepage, Olivier,Llinàs-Brunet, Montse,Naud, Julie,Poirier, Martin,Rioux, Nathalie,Thavonekham, Bounkham,Kukolj, George,Stammers, Timothy A.

, p. 4132 - 4140 (2013/07/25)

We describe the structure-based design of a novel lead chemotype that binds to thumb pocket 2 of HCV NS5B polymerase and inhibits cell-based gt1 subgenomic reporter replicons at sub-micromolar concentrations (EC50 200 nM). This new class of po

Process for preparation of substituted P-aminophenol

-

, (2013/08/28)

The present invention is related to a process of preparing substituted p-aminophenol compound of formula (I) or a salt thereof,

VIRAL POLYMERASE INHIBITORS

-

Page/Page column 68, (2009/04/25)

Compound of Formula I: wherein, R2, R5 and R6 are defined herein, are useful as inhibitors of the hepatitis C virus NS5B polymerase

VIRAL POLYMERASE INHIBITORS

-

Page/Page column 55, (2009/04/25)

Compounds of formula I: wherein X, R2, R3, R5 and R6 are defined herein, are useful as inhibitors of the hepatitis C virus NS5B polymerase.

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