CAS 143468-13-7

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

Description:

6-Bromo-1H-pyrrolo[2,3-b]pyridine is a heterocyclic organic compound characterized by its fused pyrrole and pyridine rings, with a bromine substituent at the 6-position. This compound typically exhibits a pale yellow to brown solid appearance and is soluble in organic solvents such as dimethyl sulfoxide (DMSO) and dichloromethane. It has potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its structural similarity to biologically active compounds. The presence of the bromine atom can enhance its reactivity and influence its interaction with biological targets. Additionally, 6-bromo-1H-pyrrolo[2,3-b]pyridine may exhibit interesting electronic properties due to the conjugated system formed by the fused rings, which can affect its optical characteristics. As with many heterocycles, it may also participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a valuable intermediate in organic synthesis. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity and reactivity.

Formula: C₇H₅BrN₂

InChI: InChI=1/C7H5BrN2/c8-6-2-1-5-3-4-9-7(5)10-6/h1-4H,(H,9,10)

SMILES: c1cc(Br)nc2c1cc[nH]2

Synonyms:

• 6-Bromo-7-Azaindole
• 1H-Pyrrolo[2,3-b]pyridine, 6-bromo-
• 2-Aminobenzene-1,3-Diol
• 6-Bromo-7-azaindole,96%
• 6-broMo-
• 6-broMo-1H-pyrrolo[2
• 6-BROMO-1H-PYRROLO[2,3-B]PYRIDINE

6-Bromo-7-azaindole

CAS: 143468-13-7

Formula: C₇H₅BrN₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 197.0320

Ref: IN-DA0034BY

6-Bromo-1H-pyrrolo[2,3-b]pyridine

CAS: 143468-13-7

6-Bromo-1H-pyrrolo[2,3-b]pyridine

Purity: 97%

Molecular weight: 197.03g/mol

Ref: 54-OR321485

6-Bromo-7-azaindole

CAS: 143468-13-7

Formula: C₇H₅BrN₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 197.035

Ref: 10-F076945

6-Bromo-7-azaindole

CAS: 143468-13-7

6-Bromo-7-azaindole is a homologous molecule. It is an electron deficient compound with a piperidine moiety at the 6 position and a nitrogen atom at the 7 position. The nitrogen atom substitutes for an oxygen atom, making this molecule reactive. The electron deficient nature of this molecule makes it suitable for use in transistors and other physicochemical devices. 6-Bromo-7-azaindole has been shown to be effective against carcinoma cells in vitro, as well as to inhibit tumor growth in vivo. This drug also causes homologous recombination by interacting with DNA in mammalian cells. 6-Bromo-7-azaindole binds to DNA, forming a covalent bond with the guanine base of DNA through the nitrogen atom, which is electron deficient.

Formula: C₇H₅BrN₂

Purity: Min. 95%

Color and Shape: Off-White To Beige To Yellow Solid

Molecular weight: 197.03 g/mol

Ref: 3D-FB11991