structure of 6-Bromo-1-chloronaphthalene

6-Bromo-1-chloronaphthalene

CAS No.: 1000391-24-1
M. Wt: 241.51
M. Fa: C10H6BrCl
InChI Key: KUQJGFGVAJMCNG-UHFFFAOYSA-N
Appearance: Off White Solid

Names and Identifiers of 6-Bromo-1-chloronaphthalene

CAS Number

1000391-24-1

MDL Number

MFCD18410264

IUPAC Name

6-bromo-1-chloronaphthalene

InChI

InChI=1S/C10H6BrCl/c11-8-4-5-9-7(6-8)2-1-3-10(9)12/h1-6H

InChIKey

KUQJGFGVAJMCNG-UHFFFAOYSA-N

Canonical SMILES

C1=CC2=C(C=CC(=C2)Br)C(=C1)Cl

UNSPSC Code

12352100

Physical and chemical properties of 6-Bromo-1-chloronaphthalene

H Bond Acceptors

0

H Bond Donors

0

LogP

4.33551987433333

Molecular Formula

C10H6BrCl

Molecular Weight

241.51

Storage condition

Store at room temperature

Safety Information of 6-Bromo-1-chloronaphthalene

Pictograms

Signal Word

 Warning

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

Applications of 6-Bromo-1-chloronaphthalene

6-Bromo-1-chloronaphthalene finds applications across various fields:

  • Organic Synthesis: It serves as an important building block for synthesizing more complex organic molecules.
  • Pharmaceuticals: The compound may be used in developing pharmaceutical agents due to its potential biological activity.
  • Material Science: It can be utilized in creating functional materials with specific electronic or optical properties.

Interaction Studies of 6-Bromo-1-chloronaphthalene

Interaction studies involving 6-Bromo-1-chloronaphthalene primarily focus on its reactivity with nucleophiles and electrophiles. Research indicates that its halogen substituents significantly influence its interaction profile, making it a useful intermediate for synthesizing diverse chemical entities. Studies have also examined its role in catalyzed reactions, revealing insights into reaction mechanisms and pathways .

Physical sample testing spectrum (NMR) of 6-Bromo-1-chloronaphthalene

Physical sample testing spectrum (NMR) of 6-Bromo-1-chloronaphthalene