1010073-87-6

Basic information

• Product Name: 1H-PYRAZOLO[3,4-B]PYRIDINE-3-CARBALDEHYDE
• Synonyms: 1H-PYRAZOLO[3,4-B]PYRIDINE-3-CARBALDEHYDE;1H-Pyrazolo[3,4-b]pyridine-3-carboxaldehyde;2H-pyrazolo[3,4-b]pyridine-3-carbaldehyde
• CAS NO: 1010073-87-6
• Molecular Formula: C7H5N3O
• Molecular Weight: 147
• Mol File: 1010073-87-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 383.825 °C at 760 mmHg
• Flash Point: 189.01 °C
• Appearance: /
• Density: 1.472 g/cm³
• Storage Temp.: 2-8°C
• PKA: 7.96±0.40(Predicted)
• CAS DataBase Reference: 1H-PYRAZOLO[3,4-B]PYRIDINE-3-CARBALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-PYRAZOLO[3,4-B]PYRIDINE-3-CARBALDEHYDE(1010073-87-6)
• EPA Substance Registry System: 1H-PYRAZOLO[3,4-B]PYRIDINE-3-CARBALDEHYDE(1010073-87-6)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-37/39
• Hazardous Substances Data: 1010073-87-6(Hazardous Substances Data)

Usage

General Description

1H-PYRAZOLO[3,4-B]PYRIDINE-3-CARBALDEHYDE is a chemical compound with the molecular formula C9H6N4O. It is a heterocyclic compound containing a pyrazolo-pyridine ring system and an aldehyde functional group. This chemical is used in various fields including pharmaceuticals, where it can be utilized as a building block for the synthesis of bioactive compounds. It is also used in research and development for the study of its properties and potential applications. Overall, 1H-PYRAZOLO[3,4-B]PYRIDINE-3-CARBALDEHYDE is a versatile compound with diverse potential uses in different industries.

Upstream product

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Downstream Products

• 1010073-88-7 C₂₀H₂₀ClN₅O₃ 

Relevant articles and documents

Preparation method of 1H-pyrazolo [3, 4-b] pyridine-3-formaldehyde

The invention relates to the technical field of organic synthesis, and discloses a preparation method of 1H-pyrazolo [3, 4-b] pyridine-3-formaldehyde, which comprises the following steps: S1, reacting2-fluoropyridine with 2, 2-dialkoxy acetate under the action of alkali to obtain 1-(2-fluoropyridine-3-yl)-2, 2-dialkoxy ethanone; S2, enabling the 1-(2-fluoropyridine-3-yl)-2, 2-dialkoxy ethanone toreact with hydrazine hydrate to obtain 3-(dialkoxymethyl)-1H-pyrazolo [3, 4-b] pyridine; S3, hydrolyzing the 3-(dialkoxymethyl)-1H-pyrazolo [3, 4-b] pyridine under an acidic condition to obtain 1H-pyrazolo [3, 4-b] pyridine-3-formaldehyde. The method has the advantages of readily available raw materials, low cost, convenient and safe process operation, high total yield, no need of ultra-high temperature reaction and other special equipment, high production safety factor, environmental friendliness, suitability for industrial production and the like.