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6628-28-0

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6628-28-0 Usage

Description

2-Methyl-6-ethoxyquinoline, with the molecular formula C12H13NO, is a yellow crystalline solid that serves as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals. It is recognized for its potent antimicrobial and antifungal properties, which contribute to its diverse applications across various industries.

Uses

Used in Pharmaceutical and Agrochemical Industries:
2-Methyl-6-ethoxyquinoline is used as a chemical intermediate for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and properties make it a valuable component in the development of new drugs and pesticides.
Used in Industrial and Commercial Applications:
2-Methyl-6-ethoxyquinoline is used as an antimicrobial and antifungal agent in various industrial and commercial applications. Its potent properties help to prevent the growth of harmful microorganisms, ensuring the safety and quality of products.
Used in Metalworking Fluids:
2-Methyl-6-ethoxyquinoline is used as a corrosion inhibitor in metalworking fluids. Its ability to prevent corrosion helps to extend the life of machinery and equipment, reducing maintenance costs and downtime.
Used in Perfume and Personal Care Products:
2-Methyl-6-ethoxyquinoline is used as a fragrance in the production of perfumes and personal care products. Its unique scent profile adds depth and complexity to fragrance formulations, enhancing the sensory experience for consumers.
Used in Medicinal Chemistry Research:
2-Methyl-6-ethoxyquinoline has been studied for its potential anti-inflammatory and antioxidant properties, making it a subject of interest in the field of medicinal chemistry. Its diverse pharmacological activities suggest that it may have therapeutic potential in the treatment of various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 6628-28-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6628-28:
(6*6)+(5*6)+(4*2)+(3*8)+(2*2)+(1*8)=110
110 % 10 = 0
So 6628-28-0 is a valid CAS Registry Number.
InChI:InChI=1/C28H21Cl2N3O5/c1-37-25-13-17(9-12-24(25)38-28(36)19-10-11-22(29)23(30)14-19)15-32-33-26(34)16-31-27(35)21-8-4-6-18-5-2-3-7-20(18)21/h2-15H,16H2,1H3,(H,31,35)(H,33,34)

6628-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-6-ethoxyquinoline

1.2 Other means of identification

Product number -
Other names 6-ethoxy-2-methylquinoline

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:6628-28-0 SDS

6628-28-0Relevant articles and documents

Electrophilic addition of alcohols to 1-vinyl-2-phenylazopyrroles and unexpected formation of 2-methylquinoline

Shmidt,Senotrusova,Ushakov,Protsuk,Mikhaleva,Trofimov

, p. 1495 - 1501 (2007)

1-Vinyl-2-phenylazopyrroles react with alcohols in the presence of acids or PdCl2 to give 1-(1-alkoxyethyl)-2-phenylazopyrroles in up to 49% yield. In the presence of trifluoroacetic acid 2-methylquinoline unexpectedly formed (yield up to 26%) involving into the reaction the phenylazo and 1-vinyl groups.

Facile synthesis of 2-methylquinolines from anilines on mesoporous N-doped TiO2 under UV and visible light

Selvam,Swaminathan

, p. 500 - 508 (2013/05/21)

Nitrogen-doped TiO2 was synthesized by a simple wet method using a nitrogen precursor hydrazine hydrate and nano TiO2. This photocatalyst was characterized by X-ray diffraction, highresolution transmission electron microscopy, diffused reflectance spectra, photoluminescence, and X-ray photoelectron spectroscopy. XPS analysis indicates the incorporation of anionic nitrogen in TiO2 lattice as O-Ti-N linkage. N2 adsorption-desorpion isotherm indicates the mesoporous nature of N-TiO2 with the surface area 130.0 m2/g. Sizes of N-TiO2 particles are found to be in the range of 5-30 nm by HRTEM images. DRS spectra reveal the extended absorption to the visible range. N-TiO2 is found to be more efficient than Ag-TiO2, Au-TiO2, and Pt-TiO2 in quinaldine synthesis under visible light. Copyright Taylor & Francis Group, LLC.

Au-doped TiO2 nanoparticles for selective photocatalytic synthesis of quinaldines from anilines in ethanol

Selvam,Swaminathan

scheme or table, p. 4911 - 4914 (2010/10/02)

A convenient eco-friendly photocatalytic synthesis of quinaldines has been developed by a simple one-pot reaction of anilines in ethanol solution with Au-loaded TiO2 under UV irradiation. Upon irradiation in the presence of Au-TiO2, aniline and oxidation products derived from ethanol undergo condensation-cyclization to afford quinaldines.

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