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6-Quinolinamine, 1,2,3,4-tetrahydro-2-methyl-, also known as 2-methyl-1,2,3,4-tetrahydroquinoline or 2-methyl-1,2,3,4-tetrahydro-6-quinolinamine, is an organic compound with the chemical formula C10H13N. It is a derivative of quinoline, a heterocyclic aromatic compound with a nitrogen atom in the ring. This specific compound features a methyl group attached to the 2-position of the tetrahydroquinoline structure, which is a reduced form of quinoline. It is a colorless to pale yellow liquid with a molecular weight of 149.22 g/mol. 6-Quinolinamine, 1,2,3,4-tetrahydro-2-methyl- is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique chemical structure and reactivity.

649569-61-9

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649569-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 649569-61-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,9,5,6 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 649569-61:
(8*6)+(7*4)+(6*9)+(5*5)+(4*6)+(3*9)+(2*6)+(1*1)=219
219 % 10 = 9
So 649569-61-9 is a valid CAS Registry Number.

649569-61-9SDS

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-1,2,3,4-tetrahydroquinolin-6-amine

1.2 Other means of identification

Product number -
Other names 6-Quinolinamine,1,2,3,4-tetrahydro-2-methyl

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:649569-61-9 SDS

649569-61-9Upstream product

649569-61-9Relevant academic research and scientific papers

The effect of remote chirality on the antibacterial activity of indolinyl, tetrahydroquinolyl and dihydrobenzoxazinyl oxazolidinones

Ciske, Fred L.,Barbachyn, Michael R.,Genin, Michael J.,Grega, Kevin C.,Lee, Chi Sing,Dolak, Lester A.,Seest, Eric P.,Watt, William,Adams, Wade J.,Friis, Janice M.,Ford, Charles W.,Zurenko, Gary E.

, p. 4235 - 4239 (2007/10/03)

The oxazolidinones are promising agents for the treatment of infections caused by gram-positive bacteria, including multidrug-resistant strains. In ongoing studies we have discovered that a strategically placed chiral center of appropriate absolute configuration improves the antibacterial activity of indolinyl oxazolidinone analogues (gram-positive MIC's0.5 μg/mL for the most potent congeners). The design, synthesis, antibacterial activity and pharmacokinetic profile of a selected series of α-methylated indoline derivatives and a related set of tetrahydroquinolyl and dihydrobenzoxazinyl analogues are discussed.

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