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263896-27-1

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263896-27-1 Usage

General Description

6-Ethyl-2,3-dihydroquinolin-4(1h)-one is a chemical compound belonging to the class of organic compounds known as dihydroquinolones, characterized by a quinoline moiety bearing a ketone at the fourth carbon atom. Its molecular formula is C12H13NO and has a molar mass of 189.236 g/mol. It is also identified by its systematic name, Ethylquinolin-2(1H)-one. The properties of this compound, such as solubility and boiling point, are not extensively documented. Possible uses or applications of this chemical are undetermined due to limited available data.

Check Digit Verification of cas no

The CAS Registry Mumber 263896-27-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,3,8,9 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 263896-27:
(8*2)+(7*6)+(6*3)+(5*8)+(4*9)+(3*6)+(2*2)+(1*7)=181
181 % 10 = 1
So 263896-27-1 is a valid CAS Registry Number.

263896-27-1SDS

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 6-ethyl-2,3-dihydro-1H-quinolin-4-one

1.2 Other means of identification

Product number -
Other names -

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:263896-27-1 SDS

263896-27-1Relevant articles and documents

Nanomolar inhibitors of Staphylococcus aureus methionyl tRNA synthetase with potent antibacterial activity against gram-positive pathogens

Jarvest, Richard L.,Hibbs, Martin J.,Jaworski, Deborah D.,O'Hanlon, Peter J.,Pope, Andrew J.,Rittenhouse, Stephen,Sheppard, Robert J.,Slater-Radosti, Courtney,Worby, Angela,Berge, John M.,Berry, Valerie,Boyd, Helen F.,Brown, Murray J.,Elder, John S.,Forrest, Andrew K.,Fosberry, Andrew P.,Gentry, Daniel R.

, p. 1959 - 1962 (2002)

Potent nanomolar inhibitors of Staphylococcus aureus methionyl tRNA synthetase have been derived from a file compound high throughput screening hit. Optimized compounds show excellent antibacterial activity against staphylococcal and enterococcal pathogen

METHODS OF TREATMENT OF AMYLOIDOSIS USING BI-CYCLIC ASPARTYL PROTEASE INHIBITORS

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Page/Page column 101-103; 108-109, (2010/02/14)

The invention relates to novel compounds and methods of treating diseases, disorders, and conditions associated with amyloidosis. Amyloidosis refers to a collection of diseases, disorders, and conditions associated with abnormal deposition of A-beta protein.

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