3-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridine|1190320-00-3,AngeneChemical

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-

O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]

Tris(dibenzylideneacetone)dipalladium

C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C

Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridine

Request for Quotation

Chemical Name:	3-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridine
CAS Number:	1190320-00-3
Product Number:	AG000HVZ(AGN-PC-09RUKR)
Synonyms:
MDL No:
Molecular Formula:	C7H4BrFN2
Molecular Weight:	215.0225

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
Customer Feedback

Identification/Properties

Computed Properties

Molecular Weight:

215.025g/mol

XLogP3:

2.1

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

213.954g/mol

Monoisotopic Mass:

213.954g/mol

Topological Polar Surface Area:

28.7A^2

Heavy Atom Count:

Formal Charge:

Complexity:

155

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

N/A

Signal Word:

UN#:

Hazard Statements:

Precautionary Statements:

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

Request for Quotation

Quantity Required:*

Company Name:

Contact Person:*

Email:*

Tel:*

Country:*

Others:(Optional)

Verification Code:

Customer Feedback

Chemical Structure

3-Bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridine is a versatile compound that finds significant application in chemical synthesis. It serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties and reactivity. In organic synthesis, this compound is often utilized as a valuable intermediate for the introduction of functional groups or structural motifs, enabling the creation of complex molecules with specific target properties.One of the primary uses of 3-Bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridine is in the synthesis of heterocyclic compounds, where it acts as a core scaffold for further modifications. By incorporating this compound into the molecular structure, chemists can access a diverse array of derivatives that exhibit a wide range of biological activities or material properties. Additionally, its fluorine and bromine substituents provide opportunities for selective transformations, allowing for precise control over the reactivity and selectivity of the synthetic pathway.Moreover, 3-Bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridine contributes to the development of new drugs by serving as a precursor for pharmaceutical agents targeting specific biological pathways or disease mechanisms. Its strategic placement within a molecule can enhance the pharmacokinetic profile, potency, or selectivity of the final therapeutic compound, making it a valuable tool in medicinal chemistry research.In summary, the strategic incorporation of 3-Bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridine in chemical synthesis enables the construction of diverse molecular architectures with tailored properties, making it an indispensable component in the design and production of novel compounds for various applications.