CAS 271-63-6

1H-Pirrolo[2,3-b]piridina

Descrizione:

1H-Pirrolo[2,3-b]piridina, con il numero CAS 271-63-6, è un composto organico biciclico che presenta un sistema di anelli fusi di pirrolo e piridina. Questo composto è caratterizzato dalla sua natura aromatica, che contribuisce alla sua stabilità e reattività. Appare tipicamente come un liquido o solido incolore o giallo pallido, a seconda della sua forma e purezza. La presenza di atomi di azoto in entrambi gli anelli conferisce proprietà elettroniche uniche, rendendolo di interesse in varie applicazioni chimiche e biologiche. 1H-Pirrolo[2,3-b]piridina è noto per il suo potenziale come blocco di costruzione nella sintesi di farmaci e agrochimici, così come per il suo ruolo nella chimica medicinale grazie alla sua attività biologica. Il composto può partecipare a varie reazioni chimiche, comprese sostituzioni elettrofile e aggiunte nucleofile, grazie alla natura ricca di elettroni del componente di pirrolo. La sua solubilità in solventi organici e la stabilità moderata in condizioni standard lo rendono un composto versatile nella chimica organica sintetica.

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

Sinonimi:

• 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

Purezza: >98.0%(GC)(T)

Colore e forma: White to Light yellow to Light orange powder to crystal

Peso molecolare: 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

Purezza: 98%

Colore e forma: White to cream to pale brown, Crystals or powder or crystalline powder or lumps or fused solid or flakes

Peso molecolare: 118.14

Ref: 02-L07983

7-Azaindole

CAS: 271-63-6

Formula: C₇H₆N₂

Purezza: 97%

Colore e forma: Solid

Peso molecolare: 118.1359

Ref: IN-DA0034DT

7-Azaindole

CAS: 271-63-6

7-Azaindole

Formula: C₇H₆N₂

Purezza: 98%

Colore e forma: off-white solid

Peso molecolare: 118.14g/mol

Ref: 54-OR27924

7-Azaindole

CAS: 271-63-6

7-Azaindole

Formula: C₇H₆N₂

Purezza: 98%

Colore e forma: white powder

Peso molecolare: 118.14g/mol

Ref: 54-BIA1470

7-Azaindole

CAS: 271-63-6

Formula: C₇H₆N₂

Purezza: 99.0%

Colore e forma: Solid, Chunks or Crystalline Powder

Peso molecolare: 118.139

Ref: 10-F032720

7-Azaindole

CAS: 271-63-6

Formula: C₇H₆N₂

Purezza: ≥ 98.0%

Colore e forma: White to off-white or pale yellow crystalline powder

Peso molecolare: 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

Purezza: Min. 98.0 Area-%

Peso molecolare: 118.14 g/mol

Ref: 3D-A-9500

7-Azaindole

Prodotto controllato

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

Colore e forma: Neat

Peso molecolare: 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

Colore e forma: Powder

Peso molecolare: 118.14 g/mol

Ref: 3D-FA03428