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Octahydro-2-methyl-2H-quinolizine is a cyclic amine compound with the molecular formula C10H19N. It is a colorless to pale yellow liquid with a strong, pungent odor. This chemical is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a building block in the preparation of complex organic molecules, such as alkaloids and other nitrogen-containing heterocycles. Due to its versatile chemical properties, octahydro-2-methyl-2H-quinolizine plays a significant role in the development of new drugs and chemical products.

4939-37-1

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4939-37-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4939-37-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,3 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4939-37:
(6*4)+(5*9)+(4*3)+(3*9)+(2*3)+(1*7)=121
121 % 10 = 1
So 4939-37-1 is a valid CAS Registry Number.

4939-37-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-octahydro-quinolizine

1.2 Other means of identification

Product number -
Other names 2-Methyl-chinolizidin-'A'-racemat

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:4939-37-1 SDS

4939-37-1Downstream Products

4939-37-1Relevant 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 (2007/10/03)

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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