319-04-0

Basic information

• Product Name: Naphthalene, 7-broMo-1-fluoro-
• Synonyms: Naphthalene, 7-broMo-1-fluoro-;7-Bromo-1-fluoro-naphthalene
• CAS NO: 319-04-0
• Molecular Formula: C10H6BrF
• Molecular Weight: 225.0570432
• Mol File: 319-04-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 286.6°Cat760mmHg
• Flash Point: 130.8°C
• Appearance: /
• Density: 1.563g/cm³
• Vapor Pressure: 0.00451mmHg at 25°C
• Refractive Index: 1.638
• CAS DataBase Reference: Naphthalene, 7-broMo-1-fluoro-(CAS DataBase Reference)
• NIST Chemistry Reference: Naphthalene, 7-broMo-1-fluoro-(319-04-0)
• EPA Substance Registry System: Naphthalene, 7-broMo-1-fluoro-(319-04-0)

Safety Data

• Hazardous Substances Data: 319-04-0(Hazardous Substances Data)

Usage

General Description

Naphthalene, 7-bromo-1-fluoro- is a chemical compound with the molecular formula C10H6BrF. It is a derivative of naphthalene, a polycyclic aromatic hydrocarbon, with a bromine atom and a fluorine atom attached to the seventh and first carbon atoms, respectively. Naphthalene, 7-broMo-1-fluoro- is commonly used as a starting material in the synthesis of various pharmaceuticals and agrochemicals. It can also be used as a reagent in organic synthesis and as an intermediate in the production of other organic compounds. Additionally, it has potential applications in the field of materials science, particularly in the development of new organic semiconductors and electronic devices.

InChI:InChI=1/C10H6BrF/c11-8-5-4-7-2-1-3-10(12)9(7)6-8/h1-6H

Upstream product

• 136924-78-2 1-amino-7-bromonaphthalene 
• 35943-87-4 7-bromo-1-methyl-3,4-dihydronaphthalene 
• 33295-35-1 2-bromo-8-methylnaphthalene 
• 51934-39-5 7-bromo-1-naphthalenecarboxylic acid 
• 877263-91-7 7-bromo-N-hydroxy-3,4-dihydronaphthalen-1(2H)-imine 
• 137466-04-7 7-Bromo-1-naphthylamine hydrochloride 
• 6340-79-0 4-oxo-4-(4-bromophenyl)butanoic acid 
• 35656-89-4 4-(4-bromophenyl)butanoic acid 
• 32281-97-3 7-bromo-3,4-dihydro-2H-naphthalen-1-one 
• 108-86-1 bromobenzene 
• 137466-05-8 7-Bromo-1-naphthyldiazonium tetrafluoroborate 

Downstream Products

• 2965-43-7 2-(8-Fluor-naphthoyl)-benzoesaeure 

Relevant articles and documents

SUBSTITUTED DIHYDROPYRAZOLO PYRAZINE CARBOXAMIDE DERIVATIVES

The invention relates to substituted dihydropyrazolo pyrazine carboxamide derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and diabetes, and also urogenital and ophthalmic disorders.

Nuclear Spin-Spin Coupling via Nonbonded Interactions. 7. Effects of Molecular Structure on N-F Coupling

To test wether the recently discovered phenomenon of through-space nuclear spin-spin coupling between intramolecularly crowded 15N and 19F nuclei shows the same sort of striking dependence on molecular structure as the long-known phenomenon of through-space nuclear spin-spin coupling between pairs of intramolecularly crowded 19F nuclei, several 15N-enriched oximes and some simple derivatives thereof were synthesized and their JNF values were determined by 19F NMR spectroscopy.The experimental JNF values ranged from 8.6 to 43.5 Hz.The molecular structures of these compounds were determined by single-crystal X-ray diffraction.The observed dependence of the 15N-19F coupling constants on molecular structure was qualitatively consistent with the predictions of the lone-pair orbital overlap theory that was developed earlier to account for through-space coupling involving fluorine nuclei.