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1041481-59-7

4-Fluoro-1H-indazole-5-carboxylic acid is a chemical compound with the molecular formula C8H5FN2O2. It belongs to the class of organic compounds known as indazoles, which are aromatic heterocyclic compounds containing a pyrazole ring fused to a benzene ring. 4-Fluoro-1H-indazole-5-carboxylic acid is characterized by the presence of a fluorine atom at the 4th position and a carboxylic acid group at the 5th position in the indazole ring. Known for its reactivity, 4-Fluoro-1H-indazole-5-carboxylic acid is commonly utilized in chemical synthesis processes.

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  • 1041481-59-7 Structure

  • Basic information

    1. Product Name: 4-Fluoro-1H-indazole-5-carboxylic acid
    2. Synonyms: 4-Fluoro-1H-indazole-5-carboxylic acid;5-Carboxy-4-fluoro-1H-indazole;4-Fluoro-1H-indazol-5-carboxylic acid;1H-indazole-5-carboxylic acid, 4-fluoro-
    3. CAS NO:1041481-59-7
    4. Molecular Formula: C8H5FN2O2
    5. Molecular Weight: 180.1359032
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1041481-59-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.610
    6. Refractive Index: N/A
    7. Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-Fluoro-1H-indazole-5-carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Fluoro-1H-indazole-5-carboxylic acid(1041481-59-7)
    11. EPA Substance Registry System: 4-Fluoro-1H-indazole-5-carboxylic acid(1041481-59-7)

  • 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: 1041481-59-7(Hazardous Substances Data)

1041481-59-7 Usage

Uses

Used in Chemical Synthesis:
4-Fluoro-1H-indazole-5-carboxylic acid is used as a synthetic intermediate for the production of various organic compounds and pharmaceuticals. Its unique structure and reactivity make it a valuable building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
4-Fluoro-1H-indazole-5-carboxylic acid is used as a key component in the development of new drugs. Its specific chemical properties allow it to be incorporated into the molecular structures of potential therapeutic agents, contributing to their pharmacological activity.
Used in Research and Development:
In the field of scientific research, 4-Fluoro-1H-indazole-5-carboxylic acid is employed as a research tool to study the properties and behavior of indazole-based compounds. It aids in understanding the structure-activity relationships and the potential applications of related compounds in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1041481-59-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,1,4,8 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1041481-59:
(9*1)+(8*0)+(7*4)+(6*1)+(5*4)+(4*8)+(3*1)+(2*5)+(1*9)=117
117 % 10 = 7
So 1041481-59-7 is a valid CAS Registry Number.

1041481-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Fluoro-1H-indazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names PC8937

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:1041481-59-7 SDS

1041481-59-7Relevant articles and documents

PYRAZOLE COMPOUND AND MEDICINAL COMPOSITION CONTAINING THE SAME

-

Page/Page column 86, (2008/06/13)

The present invention provides a novel compound having an excellent JNK inhibitory effect. That is, it provides a compound represented by the following formula, a salt thereof or a hydrate of them. Wherein R1 designates -(CO)h-(NRa)j-(CRb=CRc)k-Ar (wherein Ra, Rb and Rc each independently designate a hydrogen atom, a halogen atom, hydroxyl group, an optionally substituted C1-6 alkyl group or the like; Cy designates a 5- or 6-membered heteroaryl; and V each independently designate the formula -L-X-Y (wherein L designates a single bond, an optionally substituted C1-6 alkylene group or the like; X designates a single bond or the formula -A- (wherein A designates NR2, O, CO, S, SO or SO2) and so on; and Y designates a hydrogen atom, a halogen atom, nitro group or the like).

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