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1H-indazole-6-carboxylic acid

1H-indazole-6-carboxylic acid Structure
  • ₹7772.35
  • Product name: 1H-indazole-6-carboxylic acid
  • CAS: 704-91-6
  • MF: C8H6N2O2
  • MW: 162.15
  • EINECS:
  • MDL Number:MFCD06804571
  • Synonyms:INDAZOLE-6-CARBOXYLIC ACID;1H-INDAZOLE-6-CARBOXYLIC ACID;6-(1H)INDAZOLE CARBOXYLIC ACID;1H-Indazole-6-carboxylic acid 97%;1H-Indazole-6-carboxylic acid, 97%+;6-Carboxy-1H-indazole;1-H-indazole-6-carboxyle acid;1H-Indazol-6-carboxylic acid
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Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 1G
  • ManufacturerSigma-Aldrich(India)
  • Product number702420
  • Product description1H-Indazole-6-carboxylic acid 97%
  • Packaging1G
  • Price₹7772.35
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) 702420 1H-Indazole-6-carboxylic acid 97% 1G ₹7772.35 2022-06-14 Buy

Properties

Melting point :302-307 °C
Boiling point :443.7±18.0 °C(Predicted)
Density :1.506±0.06 g/cm3(Predicted)
storage temp. :Sealed in dry,Room Temperature
pka :4.01±0.30(Predicted)
form :Crystalline Powder
color :White to light brown
InChIKey :DNCVTVVLMRHJCJ-UHFFFAOYSA-N

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 May cause respiratory irritation Specific target organ toxicity, single exposure;Respiratory tract irritation Category 3 Warning GHS hazard pictograms
Precautionary statements:
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Description

1H-Indazole-6-carboxylic Acid is used as a reagent to synthesize azabicyclic aryl amides, which act as α7 nicotinic acetylcholine receptor agonists.

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