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ChemicalBook > Product Catalogue >Pharmaceutical intermediates >Heterocyclic compound >Pyridine compound >Pyridine derivatives >1H-PYRROLO[2,3-B]PYRIDIN-5-OL

1H-PYRROLO[2,3-B]PYRIDIN-5-OL

1H-PYRROLO[2,3-B]PYRIDIN-5-OL Structure
  • ₹68706.28
  • Product name: 1H-PYRROLO[2,3-B]PYRIDIN-5-OL
  • CAS: 98549-88-3
  • MF: C7H6N2O
  • MW: 134.14
  • EINECS:802-177-7
  • MDL Number:MFCD08272242
  • Synonyms:1H-PYRROLO[2,3-B]PYRIDIN-5-OL;1H-Pyrrolo[2,3-b]pyridin-5-ol(6CI,9CI);1H-Pyrrolo[2,3-b]pyridin-5-ol90929-73-0;5-Hydroxyazaindole;5-Hydroxy-7-azaindole 97%;5-hydroxypyrrolo[2,3-b]pyridine;5-HYDROXY-1H-PYRROLO[2,3-B]PYRIDINE;H-PYRROLO[2,3-B]PYRIDIN-5-OL
1 prices
Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 1G
  • ManufacturerSigma-Aldrich(India)
  • Product numberADE000886
  • Product description1H-Pyrrolo[2,3-b]pyridin-5-ol AldrichCPR
  • Packaging1G
  • Price₹68706.28
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) ADE000886 1H-Pyrrolo[2,3-b]pyridin-5-ol AldrichCPR 1G ₹68706.28 2022-06-14 Buy

Properties

Melting point :219-220°C
Boiling point :381.8±42.0 °C(Predicted)
Density :1.41±0.1 g/cm3(Predicted)
storage temp. :Keep in dark place,Sealed in dry,Room Temperature
form :Powder
pka :6.93±0.20(Predicted)
InChIKey :VUQZKLXKFUBWRP-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
H302 Harmful if swallowed Acute toxicity,oral Category 4 Warning GHS hazard pictograms P264, P270, P301+P312, P330, P501
Precautionary statements:
P280 Wear protective gloves/protective clothing/eye protection/face protection.
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-?Pyrrolo[2,?3-?b]?pyridin-?5-?ol is a reagent used in the synthesis of potent VEGFR-2 inhibitors. 7-Azaindole derivative identified as an intermediate in the synthesis of Venetoclax (A112430), a potent and selective BCL-2 inhibitor that achieves potent antitumour activity while sparing platelets.

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