66504-88-9

Basic information

• Product Name: Bicifadine Hydrochloride
• Synonyms: Bicifadine Hydrochloride;(1S,5R)-1-(4-Methylphenyl)-
• CAS NO: 66504-88-9
• Molecular Formula: C₁₂H₁₅N*ClH
• Molecular Weight: 209.71514
• Product Categories: Aromatics;Chiral Reagents;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 66504-88-9.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: Refrigerator
• Solubility: DMSO (Slightly), Methanol (Slightly)
• CAS DataBase Reference: Bicifadine Hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: Bicifadine Hydrochloride(66504-88-9)
• EPA Substance Registry System: Bicifadine Hydrochloride(66504-88-9)

Safety Data

• Hazardous Substances Data: 66504-88-9(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 66504-88-9 differently. You can refer to the following data:
1. A novel non-narcotic analgesic drug
2. Bicifadine Hydrochloride is a novel non-narcotic analgesic drug for the treatment of acute pain, chronic pain, and symptoms of neuropathic disorders.

Upstream product

• 83213-67-6 (-)-bicifadine 

Relevant articles and documents

METHODS AND COMPOSITIONS FOR PRODUCTION, FORMULATION AND USE OF 1-ARYL-3-AZABICYCLO[3.1.0] HEXANES

The invention provides novel l-aryl-3-azabicyclo[3.1.0] hexanes that are active for modulating biogenic amine transport, along with compositions and methods for using these compounds to treat central nervous system disorders. Certain l-aryl-3-azabicyclo[3.1.0] hexanes are provided that have at least one substituent on the aryl ring. In other embodiments l-aryl-3-azabicyclo[3.1.0] hexanes are provided that have a substitution on the nitrogen at the '3' position. In additional embodiments l-aryl-3-azabicyclo[3.1.0] hexanes are provided which have one substitution on the aryl ring, as well as a substitution on the nitrogen at the '3' position. The invention also provides novel methods of making aryl- and aza-substituted l-aryl-3-azabicyclo[3.1.0] hexanes, including synthetic methods that form novel intermediate compounds of the invention for producing aryl- and aza-substituted l-aryl-3-azabicyclo[3.1.0] hexanes.