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

CAS No.
98549-88-3
Chemical Name:
1H-PYRROLO[2,3-B]PYRIDIN-5-OL
Synonyms
5-HYDROXY-7-AZAINDOLE;SW-63;SWF-63;5-Hydroxyazaindole;Vinetola impurity 12;5-Hydroxy-7-azaindole 97%;H-PYRROLO[2,3-B]PYRIDIN-5-OL;1H-Pyrrolo[2,3-B]Pridin-5-ol;1H-PYRROLO[2,3-B]PYRIDIN-5-OL;5-hydroxypyrrolo[2,3-b]pyridine
CBNumber:
CB3484584
Molecular Formula:
C7H6N2O
Molecular Weight:
134.14
MDL Number:
MFCD08272242
MOL File:
98549-88-3.mol
MSDS File:
SDS
Last updated:2026-05-12 09:14:19
Product description Number Pack Size Price
1H-Pyrrolo[2,3-b]pyridin-5-ol Aldrich ADE000886 1g $870
1H-pyrrolo[2,3-b]pyridin-5-ol 97.0% P9657 1g $16
1H-pyrrolo[2,3-b]pyridin-5-ol 97.0% P9657 5g $30
1H-pyrrolo[2,3-b]pyridin-5-ol 97.0% P9657 10g $60
1H-pyrrolo[2,3-b]pyridin-5-ol 97.0% P9657 25g $150
More product size

1H-PYRROLO[2,3-B]PYRIDIN-5-OL 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
pka 6.93±0.20(Predicted)
form Powder
Appearance Light brown to light yellow Solid
InChI InChI=1S/C7H6N2O/c10-6-3-5-1-2-8-7(5)9-4-6/h1-4,10H,(H,8,9)
InChIKey VUQZKLXKFUBWRP-UHFFFAOYSA-N
SMILES C12NC=CC1=CC(O)=CN=2
UNSPSC Code 12352200

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
Hazard Codes  Xi,Xn
Risk Statements  22
Safety Statements  24/25
WGK Germany  3
HazardClass  IRRITANT
HS Code  29339900
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
REACH Registrations Active

1H-PYRROLO[2,3-B]PYRIDIN-5-OL price More Price(35)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich ADE000886 1H-Pyrrolo[2,3-b]pyridin-5-ol Aldrich 98549-88-3 1g $870 2026-04-30 Buy
Synthonix P9657 1H-pyrrolo[2,3-b]pyridin-5-ol 97.0% 98549-88-3 1g $16 2026-05-06 Buy
Synthonix P9657 1H-pyrrolo[2,3-b]pyridin-5-ol 97.0% 98549-88-3 5g $30 2026-05-06 Buy
Synthonix P9657 1H-pyrrolo[2,3-b]pyridin-5-ol 97.0% 98549-88-3 10g $60 2026-05-06 Buy
Synthonix P9657 1H-pyrrolo[2,3-b]pyridin-5-ol 97.0% 98549-88-3 25g $150 2026-05-06 Buy
Product number Packaging Price Buy
ADE000886 1g $870 Buy
P9657 1g $16 Buy
P9657 5g $30 Buy
P9657 10g $60 Buy
P9657 25g $150 Buy

1H-PYRROLO[2,3-B]PYRIDIN-5-OL Chemical Properties,Uses,Production

Chemical Properties

Light yellow solid

Uses

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.

Synthesis

5-BROMO-1-TRIISOPROPYLSILANYL-1H-PYRROLO[2,3-B]PYRIDINE

858116-66-2

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

98549-88-3

General procedure for the synthesis of 1H-pyrrolo[2,3-b]pyridin-5-ol from 1-triisopropylsilyl-5-bromo-7-azaindole: To a 50 mL reaction flask at room temperature were added the compound of formula II (4.08 g, 11.5 mmol), copper acetylacetonate (0.15 g, 0.575 mmol), MHPO (0.15 g, 0.575 mmol), lithium hydroxide monohydrate (2.42 g, 57.5 mmol), 18 mL of DMSO, and 4.5 mL of water. Stirring was turned on, the air in the reaction system was replaced with nitrogen, and the reaction temperature was raised to an internal temperature of 100°C. The reaction was maintained at this temperature for 6 h. The reaction was carried out by TLC. The progress of the reaction was monitored by TLC and after confirming that the ingredients were fully reacted, the heating was stopped and the reaction mixture was cooled to room temperature (20-30°C). 100 mL of water was added to the reaction mixture and the pH was adjusted to 6 with 2 N dilute hydrochloric acid, at which point a solid precipitated. Filtering was carried out and the solid was collected. The aqueous phase was extracted with ethyl acetate (50 mL × 3) and the organic phases were combined. The organic phase was washed sequentially with water and saturated aqueous sodium chloride solution each, and then dried over anhydrous sodium sulfate. The solvent was concentrated under reduced pressure to give the compound of formula III. Yield: 1.2 g, yield: 78.5%.

References

[1] Patent: CN107434807, 2017, A. Location in patent: Paragraph 0056-0059; 0080-0083; 0102-0106

1036007-71-2
98549-88-3
Synthesis of 1H-PYRROLO[2,3-B]PYRIDIN-5-OL from 5-Benzyloxy-1H-pyrrolo[2,3-b]pyridine
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View Lastest Price from 1H-PYRROLO[2,3-B]PYRIDIN-5-OL manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
1H-Pyrrolo[2,3-b]pyridin-5-ol pictures 2026-05-18 1H-Pyrrolo[2,3-b]pyridin-5-ol
98549-88-3
US $0.00 / kg 1kg 98% Customise Hefei Lbao Physical & Chemical Science Co.,Ltd
Venetoclax Impurity 12 pictures 2026-03-12 Venetoclax Impurity 12
98549-88-3
US $0.00 / mg 10mg 0.98 10g ShenZhen H&D Pharmaceutical Technology Co., LTD
 Venetoclax Impurity 12 pictures 2026-03-12 Venetoclax Impurity 12
98549-88-3
US $0.00-0.00 / mg 10mg 0.98 10g ShenZhen H&D Pharmaceutical Technology Co., LTD

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

5-Hydroxy-7-azaindole 97% 5-hydroxypyrrolo[2,3-b]pyridine 1H-PYRROLO[2,3-B]PYRIDIN-5-OL 1H-Pyrrolo[2,3-b]pyridin-5-ol(6CI,9CI) 5-HYDROXY-1H-PYRROLO[2,3-B]PYRIDINE H-PYRROLO[2,3-B]PYRIDIN-5-OL 5-Hydroxyazaindole 5-Hydroxy-7-azaindole Company Standards 1H-pyrrolo[2,3-b]pyridin-5-ol(For export only) SWF-63 SW-63 1H-Pyrrolo[2,3-b]pyridin-5-ol (6CI, 9CI, ACI) 1H-Pyrrolo[2,3-B]Pridin-5-ol 1H pyrrolo [2,3, B] pyridine-5-ol Vinetola impurity 12 1H-Pyrrolo[2,3-B]Pyridine-5-alcohol 5-HYDROXY-7-AZAINDOLE 98549-88-3 74420-02-4 98549-68-3 PYRIDINE