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2H-Quinolizine, octahydro-4-methyl, cis- is a chemical compound with the molecular formula C10H19N. It is a derivative of quinolizine, a bicyclic aromatic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. The octahydro prefix indicates that the compound has undergone hydrogenation, resulting in the saturation of its double bonds. The 4-methyl group signifies the presence of a methyl substituent at the fourth carbon atom, and the cis- configuration implies that the two methyl groups are located on the same side of the molecule. 2H-Quinolizine, octahydro-4-methyl-, cis- is an alkaloid, which are naturally occurring organic compounds that contain basic nitrogen atoms and are often found in plants. They are known for their diverse range of pharmacological effects and are of interest in the fields of medicine and chemistry.

6480-44-0

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6480-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6480-44-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,8 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6480-44:
(6*6)+(5*4)+(4*8)+(3*0)+(2*4)+(1*4)=100
100 % 10 = 0
So 6480-44-0 is a valid CAS Registry Number.

6480-44-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R,9aR)-4-methyl-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizine

1.2 Other means of identification

Product number -
Other names 2H-Quinolizine,octahydro-4-methyl-,cis

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:6480-44-0 SDS

6480-44-0Relevant academic research and scientific papers

Synthesis of trans-2,6-Dialkylpiperidines by Intramolecular Amidomercuration

Carruthers, William,Williams, Michael J.,Cox, Michael T.

, p. 1235 - 1236 (1984)

Intramolecular amidomercuration of N-methoxycarbonyl-6-aminohept-1-ene and reaction of the resulting organomercurial with sodium borohydride in the presence of acrylonitrile or decen-3-one has been used to prepare trans-2,6-dialkylpiperidines, including solenopsin A, a constituent of the venom of the fire-ant.

Hydroformylation of alkenylamines. Concise approaches toward piperidines, quinolizidines, and related alkaloids

Airiau, Etienne,Girard, Nicolas,Pizzeti, Marianna,Salvadori, Jessica,Taddei, Maurizio,Mann, Andre

supporting information; experimental part, p. 8670 - 8673 (2011/02/28)

Linear hydroformylation of N-protected allyl- or homoallylamines (cyclohydrocarbonylation: CHC), followed by a reductive amination constitute the two key steps toward convenient routes to aza-heterocycles.

Novel synthesis of indolizidines and quinolizidines

Tehrani, Kourosch Abbaspour,D'hooghe, Matthias,De Kimpe, Norbert

, p. 3099 - 3108 (2007/10/03)

A very short synthesis of indolizidines, quinolizidines and some higher homologues was developed by alkylation of 2-methyl-1-pyrroline or 6-methyl-2,3,4,5-tetrahydropyridine with 1,3- or 1,4-dihaloalkanes, followed by reduction of the intermediate iminium salts, resulting in the desired 1-azabicyclo[m.n.0]alkanes in good yields.

Synthesis of trans-2,6-Dialkylpiperidines by Intramolecular Amidomercuriation and by 1,3-Cycloaddition of Alkenes to 2-Methyl-2,3,4,5-tetrahydropyridine Oxide

Adams, David R.,Carruthers, William,Williams, Michael J.,Crowley, Patrick J.

, p. 1507 - 1513 (2007/10/02)

Intramolecular amidomercuriation of methyl N-hept-6-en-2-ylcarbamate and reaction of the resulting organomercurial with sodium borohydride in the presence of acrylonitrile or dec-1-en-3-one has been used to prepare trans-2,6-dialkylpiperidines.A more stereoselective route lies in the cycloaddition of alkenes to 2-alkyl-2,3,4,5-tetrahydropyridine oxides followed by reductive cleavage of the resulting perhydroisoxazolopyridine.Both procedures are illustrated by synthesis of the fire ant-venom alkaloid, solenopsin A.

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