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Benzenamine, N-1-azabicyclo[2.2.2]oct-3-ylidene-, also known as 1-(1-Azabicyclo[2.2.2]oct-3-ylidene)benzenamine, is an organic compound with the chemical formula C13H18N2. It is a derivative of benzenamine (aniline) and 1-azabicyclo[2.2.2]octane, featuring a nitrogen atom in the bicyclic ring structure. Benzenamine, N-1-azabicyclo[2.2.2]oct-3-ylidene- is characterized by its unique molecular structure, which includes a benzene ring connected to a nitrogen atom within a bicyclic ring system. It is used in various chemical reactions and synthesis processes, particularly in the pharmaceutical and chemical industries, due to its potential applications in the development of drugs and other chemical compounds.

6530-15-0

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6530-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6530-15-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,3 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6530-15:
(6*6)+(5*5)+(4*3)+(3*0)+(2*1)+(1*5)=80
80 % 10 = 0
So 6530-15-0 is a valid CAS Registry Number.

6530-15-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenyl-1-azabicyclo[2.2.2]octan-3-imine

1.2 Other means of identification

Product number -
Other names (1-aza-bicyclo[2.2.2]oct-3-ylidene)-phenyl-amine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6530-15-0 SDS

6530-15-0Relevant academic research and scientific papers

SPIRO-OXADIAZOLINE COMPOUNDS AS AGONISTS OF α-7-NICOTINIC ACETYLCHOLINE RECEPTORS

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Paragraph 00598-00599, (2015/05/19)

The present invention relates to novel spiro-oxadiazoline compounds that are suitable as agonists or partial agonists of a7-nAChR, and pharmaceutical compositions of the same, methods of preparing these compounds and compositions, and the use of these compounds and compositions in methods of maintaining, treating and/or improving cognitive function. In particular, methods of administering a spiro-oxadiazoline cx7-nAChR agonist or partial agonist, to a patient in need thereof, for example a patient with a cognitive deficiency and/or a desire to enhance cognitive function, that may derive a benefit therefrom.

SUBSTITUTED AMINOQUINUCLIDINE COMPOUNDS

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Page 19, (2010/02/06)

This invention is directed towards substituted aminoquinuclidine compounds useful as delta-opioid receptor modulators, delta-opioid receptor agonists useful as analgesics and delta-opioid receptor antagonists useful as immunosuppressants, antiinflammatory agents, agents for the treatment of neurological and psychiatric conditions, medicaments for drug and alcohol abuse, agents for treating gastritis and diarrhea, cardiovascular agents and agents for the treatment of respiratory diseases.

PROCESS FOR HYDROGENATING UNACTIVATED IMINES USING RUTHENIUM COMPLEXES AS CATALYSTS

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Page/Page column 16-17; 20, (2008/06/13)

A process is provided for the hydrogenation or asymmetric hydrogenation of dialkyl, alkylalkenyl and dialkenyl imines of formula (II) to provide amines of formula (III), wherein, (i) R1 and R2 are optionally substituted cyclic, linear or branched alkyl or alkenyl; R3 is a hydrogen atom, a hydroxy radical, optionally substituted C1 to C8 cyclic, linear or branched alkyl or alkenyl, optionally substituted aryl; or (ii) R1 is alkyl or alkenyl, R2 is alkyl or alkenyl and the two are linked together or with R3 to form one or more rings; using a catalytic system comprising a base and a ruthenium complex containing (1) a diamine and (2) a diphosphine ligand or monodentate phosphine ligands in hydrogenation and asymmetric hydrogenation processes.

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