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2H-Quinolizine, octahydro-2-methyl, cis- is a chemical compound with the molecular formula C10H19N. It belongs to the class of quinolines, which are heterocyclic aromatic compounds containing a nitrogen atom in the ring structure. This specific compound features an octahydroquinolizine core, which means it has a saturated six-membered ring with two additional hydrogen atoms attached to it. The presence of a methyl group (-CH3) at the 2-position and the cis-configuration indicates that the double bond is in a specific geometric arrangement, with the substituents on the same side of the molecule. 2H-Quinolizine, octahydro-2-methyl-, cis- is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its role as an intermediate in organic chemistry.

5581-90-8

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5581-90-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5581-90-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,8 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5581-90:
(6*5)+(5*5)+(4*8)+(3*1)+(2*9)+(1*0)=108
108 % 10 = 8
So 5581-90-8 is a valid CAS Registry Number.

5581-90-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,9aR)-2-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-2-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:5581-90-8 SDS

5581-90-8Downstream Products

5581-90-8Relevant academic research and scientific papers

Determining the Scope of the Organolanthanide-Catalyzed, Sequential Intramolecular Amination/Cyclization Reaction: Formation of Substituted Quinolizidines, Indolizidines, and Pyrrolizidines

Molander, Gary A.,Pack, Shawn K.

, p. 9214 - 9220 (2003)

The scope of the lanthanide-mediated, intramolecular amination/cyclization reaction was determined for the formation of substituted quinolizidines, indolizidines, and pyrrolizidines. A methyl group was installed at diverse positions in the substrates to d

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