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Quinoline, 4,6,7-trimethyl- is an organic compound with the chemical formula C12H11N. It is a derivative of quinoline, a heterocyclic aromatic compound consisting of a benzene ring fused to a pyridine ring. The 4,6,7-trimethyl substitution refers to the presence of three methyl groups (CH3) attached to the quinoline molecule at the 4th, 6th, and 7th positions. Quinoline, 4,6,7-trimethyl- is known for its yellow crystalline appearance and is soluble in organic solvents. It is synthesized through various methods, including the condensation of acetaldehyde with malononitrile in the presence of ammonia, followed by a series of reactions. Quinoline, 4,6,7-trimethyl- has potential applications in the pharmaceutical and chemical industries, particularly as an intermediate in the synthesis of various compounds. Due to its complex structure and potential reactivity, it is important to handle Quinoline, 4,6,7-trimethyl- with care, following proper safety protocols.

6804-16-6

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6804-16-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6804-16-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,0 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6804-16:
(6*6)+(5*8)+(4*0)+(3*4)+(2*1)+(1*6)=96
96 % 10 = 6
So 6804-16-6 is a valid CAS Registry Number.

6804-16-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6,7-trimethylquinoline

1.2 Other means of identification

Product number -
Other names Quinoline,4,6,7-trimethyl

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:6804-16-6 SDS

6804-16-6Relevant academic research and scientific papers

Stabilized Ru[(H2O)6]3+ in Confined Spaces (MOFs and Zeolites) Catalyzes the Imination of Primary Alcohols under Atmospheric Conditions with Wide Scope

Mon, Marta,Adam, Rosa,Ferrando-Soria, Jesús,Corma, Avelino,Armentano, Donatella,Pardo, Emilio,Leyva-Pérez, Antonio

, p. 10401 - 10406 (2018/10/24)

Imines are ubiquitous intermediates in organic synthesis, and the metal-mediated imination of alcohols is one of the most direct and simple methods for their synthesis. However, reported protocols lack compatibility with many other functional groups since basic supports/media, pure oxygen atmospheres, and/or released hydrogen gas are required during reaction. Here we show that, in contrast to previous metal-catalyzed methods, hexa-aqueous Ru(III) catalyzes the imination of primary alcohols with very wide functional group tolerance, at slightly acid pH and under low oxygen atmospheres. The inorganic metal complex can be supported and stabilized, integrally, within either faujasite-type zeolites (Y and X) or a metal organic framework (MOF), to give a reusable heterogeneous catalyst which provides an industrially viable process well below the flammability limit of alcohols and amines.

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