CAS 271-63-6

1H-Pyrrolo[2,3-b]pyridine

Description:

1H-Pyrrolo[2,3-b]pyridine, with the CAS number 271-63-6, is a bicyclic organic compound that features a fused pyrrole and pyridine ring system. This compound is characterized by its aromatic nature, which contributes to its stability and reactivity. It typically appears as a colorless to pale yellow liquid or solid, depending on its form and purity. The presence of nitrogen atoms in both rings imparts unique electronic properties, making it of interest in various chemical and biological applications. 1H-Pyrrolo[2,3-b]pyridine is known for its potential as a building block in the synthesis of pharmaceuticals and agrochemicals, as well as its role in medicinal chemistry due to its biological activity. The compound can participate in various chemical reactions, including electrophilic substitutions and nucleophilic additions, owing to the electron-rich nature of the pyrrole component. Its solubility in organic solvents and moderate stability under standard conditions make it a versatile compound in synthetic organic chemistry.

Formula: C₇H₆N₂

InChI: InChI=1S/C7H6N2/c1-2-6-3-5-9-7(6)8-4-1/h1-5H,(H,8,9)

InChI key: InChIKey=MVXVYAKCVDQRLW-UHFFFAOYSA-N

SMILES: C1=2C(NC=C1)=NC=CC2

Synonyms:

• 1,7-Diazaindene
• 1,7-Dideazapurine
• 1H-Pyrrole[2,3-b]pyridine
• 1H-Pyrrolo[2,3-b]pyridine
• 7-Aza-1-pyrindine
• 7H-Pyrrolo[2,3-b]pyridine
• NSC 67063
• NSC 77951
• 7-Azaindole

1H-Pyrrolo[2,3-b]pyridine

CAS: 271-63-6

Formula: C₇H₆N₂

Purity: >98.0%(GC)(T)

Color and Shape: White to Light yellow to Light orange powder to crystal

Molecular weight: 118.14

Ref: 3B-P1117

7-Azaindole, 98%

CAS: 271-63-6

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₇H₆N₂

Purity: 98%

Color and Shape: White to cream to pale brown, Crystals or powder or crystalline powder or lumps or fused solid or flakes

Molecular weight: 118.14

Ref: 02-L07983

7-Azaindole

CAS: 271-63-6

Formula: C₇H₆N₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 118.1359

Ref: IN-DA0034DT

7-Azaindole

CAS: 271-63-6

7-Azaindole

Formula: C₇H₆N₂

Purity: 98%

Color and Shape: off-white solid

Molecular weight: 118.14g/mol

Ref: 54-OR27924

7-Azaindole

CAS: 271-63-6

7-Azaindole

Formula: C₇H₆N₂

Purity: 98%

Color and Shape: white powder

Molecular weight: 118.14g/mol

Ref: 54-BIA1470

7-Azaindole

CAS: 271-63-6

Formula: C₇H₆N₂

Purity: 99.0%

Color and Shape: Solid, Chunks or Crystalline Powder

Molecular weight: 118.139

Ref: 10-F032720

7-Azaindole

CAS: 271-63-6

Formula: C₇H₆N₂

Purity: ≥ 98.0%

Color and Shape: White to off-white or pale yellow crystalline powder

Molecular weight: 118.14

Ref: 7W-GK7272

7-Azaindole

CAS: 271-63-6

7-Azaindole is a chemical compound that can be used as a building block in organic synthesis. It can be used as a reactant in the preparation of other chemicals, such as dyes, rubber accelerators, and pharmaceuticals. 7-Azaindole is also useful as an intermediate in the production of polymers, such as polyurethanes and polyesters. This chemical is soluble in water and alcohols, but insoluble in ethers and chloroform. 7-Azaindole has been classified by the International Agency for Research on Cancer (IARC) as Group 3: Not Classifiable as to its Carcinogenicity to Humans.

Formula: C₇H₆N₂

Purity: Min. 98.0 Area-%

Molecular weight: 118.14 g/mol

Ref: 3D-A-9500

7-Azaindole

Controlled Product

CAS: 271-63-6

Applications Imidazolinone derivatives as CGRP receptor antagonists used in the treatment of migraine.
References Sikazwe, D., et al.: Bioorg. Med. Chem., 17, 1716 (2009), Stump, C., et al.: Bioorg. Med. Chem. Lett., 19, 214 (2009),

Formula: C₇H₆N₂

Color and Shape: Neat

Molecular weight: 118.14

Ref: TR-A800275

7-Azaindole

CAS: 271-63-6

7-Azaindole is a reactive chemical that has been shown to be effective in the treatment of skin cancer, as well as hepatic steatosis. The compound can promote the transfer of hydrogen atoms and form a dimer with protonated nitrogen. 7-Azaindole reacts rapidly with nucleophiles such as amines, alcohols, and thiols to form covalent bonds. The reaction mechanism is characterized by an initial protonation step followed by nucleophilic attack or hydrogen transfer from the nucleophile to 7-azaindole. Kinetic studies have demonstrated that the rate of this reaction depends on the concentration of both reactants.

Formula: C₇H₆N₂

Color and Shape: Powder

Molecular weight: 118.14 g/mol

Ref: 3D-FA03428