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68262-44-2

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68262-44-2 Usage

Chemical structure

A complex organic compound with a triaza-dien-ium structure.

Quinoline ring

Contains a quinoline ring, which is a common structural motif in many bioactive compounds.

Chloro substitution

The quinoline ring has a chloro substitution at the 7th position, which can influence the compound's reactivity and properties.

Ethoxycarbonyl group

An ethoxycarbonyl group is present at the 3rd position of the quinoline ring, which can provide additional functional groups for further reactions or modifications.

Triaza-dien-ium moiety

The molecule contains a nitrogen-containing three-membered ring connected to a diene structure, which contributes to its unique and potentially reactive properties.

Potential applications

May have applications in pharmaceuticals, materials science, or organic synthesis due to the presence of the quinoline and triaza-dien-ium moieties.

Structural complexity

The compound's structural complexity makes it an interesting target for further research and development.

Potential reactivity

The presence of the triaza-dien-ium moiety and the chloro substitution can lead to unique reactivity, which can be exploited in various chemical reactions and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 68262-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,6 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 68262-44:
(7*6)+(6*8)+(5*2)+(4*6)+(3*2)+(2*4)+(1*4)=142
142 % 10 = 2
So 68262-44-2 is a valid CAS Registry Number.

68262-44-2SDS

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 ethyl 4-azido-7-chloroquinoline-3-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl-4-azido-7-chloroquinoline-3-carboxylate

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:68262-44-2 SDS

68262-44-2Downstream Products

68262-44-2Relevant articles and documents

Synthesis of new quinoline fused heterocycles such as benzo[h]-1,6- naphthyridines and pyrazolo[4,3 c]quinolines

Ghotekar, Bhausaheb Kedarnath,Ghagare, Maruti G.,Toche, Raghunath B.,Jachak, Madhukar N.

experimental part, p. 169 - 175 (2010/08/05)

Synthesis of novel benzo[h]-1,6-naphthyridines was successfully achieved by cyclocondensation of ethyl 4-aminoquinoline-3-carboxylates with malononitrile. The pyrazolo[4,3-c]quinolines were synthesized by nucleophilic substitution and subsequent addition

Penicillins

-

, (2008/06/13)

New penicillin antibiotics are disclosed which are effective antibacterial agents and which belong to the class of α-(heterocyclic acylamino) penicillins and their salts and esters together with pharmaceutical compositions containing the same and their method of administration. The new compounds are characterized by having an amino substituent on the heterocyclic ring which is linked through an acylamino group to the α-carbon atom of the penicillin side chain. Procedure for preparing the new penicillins is described as well as the antibacterial activity of exemplary compounds against typical microorganisms.

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