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1H-Indazole-5-carboxylic acid, 3-formylis a chemical compound derived from the indazole family. It is characterized by the presence of a formyl group at the 3-position and a carboxylic acid group at the 5-position of the indazole ring. 1H-Indazole-5-carboxylicacid,3-forMylhas potential applications in various fields due to its unique chemical properties and structure.

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  • 885519-98-2 Structure
  • Basic information

    1. Product Name: 1H-Indazole-5-carboxylicacid,3-forMyl-
    2. Synonyms: 1H-Indazole-5-carboxylicacid,3-forMyl-;3-ForMyl-1H-indazole-5-carboxylic;3-Formyl-5-indazole carbocylic acid
    3. CAS NO:885519-98-2
    4. Molecular Formula: C9H6N2O3
    5. Molecular Weight: 190.15554
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 885519-98-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 521.9±30.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.594±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. PKA: 3.76±0.30(Predicted)
    10. CAS DataBase Reference: 1H-Indazole-5-carboxylicacid,3-forMyl-(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1H-Indazole-5-carboxylicacid,3-forMyl-(885519-98-2)
    12. EPA Substance Registry System: 1H-Indazole-5-carboxylicacid,3-forMyl-(885519-98-2)
  • 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: 885519-98-2(Hazardous Substances Data)

885519-98-2 Usage

Uses

Used in Pharmaceutical Industry:
1H-Indazole-5-carboxylic acid, 3-formylis used as a kinase inhibitor for the development of therapeutic agents. Kinase inhibitors are a class of drugs that target specific enzymes involved in cellular signaling pathways, playing a crucial role in the regulation of various cellular processes, including cell growth, differentiation, and apoptosis. By inhibiting the activity of these enzymes, 1H-Indazole-5-carboxylic acid, 3-formylcan potentially be used in the treatment of various diseases, such as cancer and inflammatory disorders.
Used in Chemical Synthesis:
1H-Indazole-5-carboxylic acid, 3-formylcan also be used as a building block or intermediate in the synthesis of more complex organic compounds. Its unique structure and functional groups make it a valuable component in the development of new pharmaceuticals, agrochemicals, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 885519-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,5,1 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 885519-98:
(8*8)+(7*8)+(6*5)+(5*5)+(4*1)+(3*9)+(2*9)+(1*8)=232
232 % 10 = 2
So 885519-98-2 is a valid CAS Registry Number.
InChI:InChI=1S/C9H6N2O3/c12-4-8-6-3-5(9(13)14)1-2-7(6)10-11-8/h1-4H,(H,10,11)(H,13,14)

885519-98-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-formyl-2H-indazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1H-Indazole-5-carboxylic acid,3-forMyl

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:885519-98-2 SDS

885519-98-2Upstream product

885519-98-2Downstream Products

885519-98-2Relevant articles and documents

An optimized procedure for direct access to 1: H -indazole-3-carboxaldehyde derivatives by nitrosation of indoles

Chevalier, Arnaud,Ouahrouch, Abdelaaziz,Arnaud, Alexandre,Gallavardin, Thibault,Franck, Xavier

, p. 13121 - 13128 (2018/04/23)

Indazole derivatives are currently drawing more and more attention in medicinal chemistry as kinase inhibitors. 1H-indazole-3-carboxaldehydes are key intermediates to access to a variety of polyfunctionalized 3-substituted indazoles. We report here a general access to this motif, based on the nitrosation of indoles in a slightly acidic environment. These very mild conditions allow the conversion of both electron-rich and electron-deficient indoles into 1H-indazole-3-carboxaldehydes.

SUBSTITUTED INDAZOLE DERIVATIVES, THEIR MANUFACTURE AND USE AS PHARMACEUTICAL AGENTS

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Page/Page column 35, (2008/06/13)

Objects of the present invention are the compounds of formula (I) their pharmaceutically acceptable salts, enantiomeric forms, diastereoisomers and racemates, the preparation of the above-mentioned compounds, medicaments containing them and their manufact

Tricyclic heterocycles

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Page/Page column 39, (2008/06/13)

The present invention relates to the compounds of formula I their pharmaceutically acceptable salts or esters, enantiomeric forms, diastereoisomers and racemates, the preparation of the above-mentioned compounds, pharmaceutical compositions containing suc

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