structure of 6-Bromo-3-iodo-1H-pyrrolo[3,2-c]pyridine

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

CAS No.: 1000341-73-0
M. Wt: 322.928
M. Fa: C7H4BrIN2
InChI Key: FCXXMGLYWFECRW-UHFFFAOYSA-N
Appearance: White Solid

Names and Identifiers of 1000341-73-0

CAS Number

1000341-73-0

MDL Number

MFCD09749987

IUPAC Name

6-bromo-3-iodo-1H-pyrrolo[3,2-c]pyridine

InChI

InChI=1S/C7H4BrIN2/c8-7-1-6-4(2-11-7)5(9)3-10-6/h1-3,10H

InChIKey

FCXXMGLYWFECRW-UHFFFAOYSA-N

Canonical SMILES

C1=C2C(=CN=C1Br)C(=CN2)I

UNSPSC Code

12352100

Physical and chemical properties of 1000341-73-0

Boiling Point

438.7±40.0 °C at 760 mmHg

Density

2.4±0.1 g/cm3

Exact Mass

321.860229

Flash Point

219.1±27.3 °C

H Bond Acceptors

1

H Bond Donors

1

Index of Refraction

1.804

LogP

2.49

Molecular Formula

C7H4BrIN2

Molecular Weight

322.928

PSA

28.68000

Storage condition

2-8°C

Vapour Pressure

0.0±1.0 mmHg at 25°C

Safety Information of 1000341-73-0

Pictograms

Signal Word

 Warning

Safety Data Sheet
Supports customized editing of SDS information and downloading in PDF documents.

Applications of 1000341-73-0

6-Bromo-3-iodo-1H-pyrrolo[3,2-c]pyridine serves as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals. Its unique structure allows it to be a precursor for various bioactive compounds. Additionally, it may find applications in materials science due to its electronic properties .

Interaction Studies of 1000341-73-0

Studies on the interactions of 6-bromo-3-iodo-1H-pyrrolo[3,2-c]pyridine with biological targets have indicated its potential role as a modulator in biochemical pathways. Its inhibitory effects on xanthine oxidase highlight its relevance in research focused on gout and related metabolic disorders . Further investigation into its interaction with other enzymes could provide insights into its therapeutic potential.

Biological Activity of 1000341-73-0

Research indicates that 6-bromo-3-iodo-1H-pyrrolo[3,2-c]pyridine exhibits significant biological activity. It has been studied for its potential as an inhibitor of xanthine oxidase, an enzyme involved in purine metabolism. Preliminary findings suggest it acts as a weak, non-competitive inhibitor of this enzyme . Additionally, compounds with similar structures have shown promise in various therapeutic areas, including anti-inflammatory and anticancer activities.

Physical sample testing spectrum (NMR) of 1000341-73-0

Physical sample testing spectrum (NMR) of 1000341-73-0

Retrosynthesis analysis of 1000341-73-0

  • Route#1

    Cas:1000342-71-1
    Cas:1000341-73-0