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1-allyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione is a heterocyclic compound characterized by its complex and unique structure. It features an allyl group attached to a pyrido-oxazine ring system, which endows it with potential applications in various fields of chemistry, particularly organic synthesis and medicinal chemistry. 1-allyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione's specific properties and potential uses are areas that require further exploration and research.

97484-75-8

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97484-75-8 Usage

Uses

Used in Organic Synthesis:
1-allyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione is used as a building block in organic synthesis for its ability to contribute to the formation of complex molecular structures. Its unique structural features make it a valuable component in the creation of novel chemical compounds.
Used in Medicinal Chemistry:
1-allyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione is used as a potential candidate in the development of new drugs due to its distinctive chemical properties. 1-allyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione may play a role in the design and synthesis of pharmaceutical agents, particularly those targeting specific biological pathways or diseases.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-allyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione is used as a precursor or intermediate in the synthesis of various drug molecules. Its unique structural elements can be leveraged to create new therapeutic agents with improved efficacy and selectivity.
Used in Chemical Research:
1-allyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione is utilized in chemical research as a subject of study to better understand its properties, reactivity, and potential applications. Researchers may investigate its behavior in various chemical reactions and its interactions with other molecules to uncover new uses and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 97484-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,4,8 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97484-75:
(7*9)+(6*7)+(5*4)+(4*8)+(3*4)+(2*7)+(1*5)=188
188 % 10 = 8
So 97484-75-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O3/c1-2-6-12-8-7(4-3-5-11-8)9(13)15-10(12)14/h2-5H,1,6H2

97484-75-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-prop-2-enylpyrido[2,3-d][1,3]oxazine-2,4-dione

1.2 Other means of identification

Product number -
Other names N-allyl-3-azaisatoic anhydride

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:97484-75-8 SDS

97484-75-8Upstream product

97484-75-8Downstream Products

97484-75-8Relevant academic research and scientific papers

Anti-infective agents

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Page/Page column 85, (2010/02/08)

The present invention provides an HCV polymerase inhibiting compound having the formula (I) and a composition comprising a therapeutically effective amount of said compound. The present invention also provides a method for inhibiting hepatitis C virus (HC

Anti-infective agents

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, (2008/06/13)

Compounds having the formula are hepatitis C(HCV) polymerase inhibitors. Also disclosed are a composition and method for inhibiting hepatitis C(HCV) polymerase, processes for making the compounds, and synthetic intermediates employed in the processes.

Anti-infective agents

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Page 52, (2010/02/06)

Compounds having the formula are hepatitis C (HCV) polymerase inhibitors. Also disclosed are a composition and method for inhibiting hepatitis C (HCV) polymerase, processes for making the compounds, and synthetic intermediates employed in the processes.

The Chemistry of 3-Azaisatoic Anhydrides. Synthesis and Reactions of Polyaza Heterocycles

Coppola, Gary M.,Fraser, James D.,Hardtmann, Goetz E.,Shapiro, Michael J.

, p. 193 - 206 (2007/10/02)

The preparation of a variety of N-substituted 3-azaisotoic anhydrides 3 and 8 is described.These anhydrides reacted with thiopseudoureas to give interesting bicyclic, tricyclic, and tetracyclic heterocycles many of which are new ring systems.One such hete

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