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2,3-Dihydro-2-oxo-1H-pyrido[2,3-b][1,4]oxazine-7-carboxylic Acid is a pyridyl analogue of 3-Oxo-3,4-dihydro-2H-1,4-(benzothiazine or benzoxazine)-6-carbaldehydes, characterized by its unique chemical structure and properties. It is a compound of interest in the field of medicinal chemistry, particularly for its potential applications in the development of new drugs and therapies.

615568-49-5

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615568-49-5 Usage

Uses

Used in Pharmaceutical Industry:
2,3-Dihydro-2-oxo-1H-pyrido[2,3-b][1,4]oxazine-7-carboxylic Acid is used as a key compound in the development of new drugs for antibacterial applications. Its unique chemical structure allows it to target specific bacterial mechanisms, potentially leading to the creation of more effective and targeted treatments for bacterial infections.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2,3-Dihydro-2-oxo-1H-pyrido[2,3-b][1,4]oxazine-7-carboxylic Acid serves as an important research tool. Scientists and researchers utilize 2,3-Dihydro-2-oxo-1H-pyrido[2,3-b][1,4]oxazine-7-carboxylic Acid to study its interactions with various biological targets, which can provide valuable insights into the development of novel antibacterial drugs and therapies.
Used in Drug Design and Development:
The unique properties of 2,3-Dihydro-2-oxo-1H-pyrido[2,3-b][1,4]oxazine-7-carboxylic Acid make it a valuable asset in the process of drug design and development. Its structure can be modified and optimized to create new drug candidates with improved efficacy, selectivity, and safety profiles, ultimately contributing to the advancement of antibacterial medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 615568-49-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,5,5,6 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 615568-49:
(8*6)+(7*1)+(6*5)+(5*5)+(4*6)+(3*8)+(2*4)+(1*9)=175
175 % 10 = 5
So 615568-49-5 is a valid CAS Registry Number.

615568-49-5SDS

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-Oxo-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine-7-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Oxo-2,3-dihydro-1H-benzoimidazole-5-sulfonyl chloride

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:615568-49-5 SDS

615568-49-5Downstream Products

615568-49-5Relevant articles and documents

The design of efficient and selective routes to pyridyl analogues of 3-oxo-3,4-dihydro-2H-1,4-(benzothiazine or benzoxazine)-6-carbaldehydes

Brooks, Gerald,Dabbs, Steven,Davies, David T.,Hennessy, Alan J.,Jones, Graham E.,Markwell, Roger E.,Miles, Timothy J.,Owston, Nathan A.,Pearson, Neil D.,Peng, Tony W.

scheme or table, p. 5035 - 5037 (2011/01/04)

This Letter describes the synthesis of challenging pyridyl analogues of 3-oxo-3,4-dihydro-2H-1,4-(benzothiazine or benzoxazine)-6-carbaldehydes. The six different routes described are high yielding, contain no major purification issues and have been used to give gram quantities of each aldehyde.

ANTIBACTERIAL AGENTS

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Page/Page column 42, (2010/11/25)

Naphthalene, quinoline, quinoxaline and naphthyridine derivatives useful in the treatment of bacterial infections in mammals, particularly humans, are disclosed herein.

NITROGEN-CONTAINING BICYCLIC HETEROCYCLES FOR USE AS ANTIBACTERIALS

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Page/Page column 84, (2010/02/07)

Cyclohexane and cyclohexene derivatives and pharmaceutically acceptable derivatives hereof useful in methods of treatment of bacterial infections in mammals, particularly man.

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