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8-Nitro-2,4-dimethylquinoline is a chemical compound with the molecular formula C11H10N2O2. It is a derivative of quinoline, a heterocyclic aromatic compound, and features a nitro group at the 8th position, and two methyl groups at the 2nd and 4th positions. This yellow crystalline solid is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and dyes. Due to its potential applications in the production of antimalarial drugs, it has gained significant attention in the field of medicinal chemistry. However, it is important to note that 8-nitro-2,4-dimethylquinoline may have toxic properties, and proper handling and safety measures should be taken when working with 8-Nitro-2,4-dimethylquinoline.

2801-28-7

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2801-28-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2801-28-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2801-28:
(6*2)+(5*8)+(4*0)+(3*1)+(2*2)+(1*8)=67
67 % 10 = 7
So 2801-28-7 is a valid CAS Registry Number.

2801-28-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dimethyl-8-nitro-quinoline

1.2 Other means of identification

Product number -
Other names 8-Nitro-2,4-dimethyl-chinolin

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:2801-28-7 SDS

2801-28-7Downstream Products

2801-28-7Relevant academic research and scientific papers

Transition-Metal-Free Regioselective C–H Bond Fluorination of 8-Amidoquinolines with Selectfluor

Chen, Hao,Li, Pinhua,Wang, Min,Wang, Lei

supporting information, p. 2091 - 2097 (2018/05/31)

A simple and efficient transition-metal-free protocol for the regioselective C–H bond fluorination of 8-aminoquinoline scaffolds with Selectfluor was developed. The reaction has a broad substrate scope and provides facile access to the corresponding C-5 f

A 1H and 13C NMR Spectral Study of the TONIC and peri-Proximity Effects in some Methylnitroquinolines and a Re-examination of the Nitration of 2,4-Dimethylquinone

Osborne, Alan G.,Hurst, Lee J.

, p. 1327 - 1366 (2007/10/03)

A NMR spectral study of some 4-methyl-5-nitro-quinoline derivatives is reported. In the proton spectrum, characteristic reduced deshielding effects are observed at H-6 as a consequence of the TONIC (Twisted Orthogonal Nitro Induced Chemical shift) effect. The peri-proximity effect for the Me/NO2 couple in 13C NMR is dominated by the rotation of the nitro group. Comparisons with the Me/Me and NO2/NO2 peri-couples are made. Nitration of 2,4-dimethylquinoline gives the 5-, 6- and 8-nitrocompounds in the ratio 13:26:61.

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