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200195-19-3

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  • SAGECHEM/3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-carbaldehyde/SAGECHEM/Manufacturer in China

    Cas No: 200195-19-3

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200195-19-3 Usage

Description

3-OXO-3,4-DIHYDRO-2H-BENZO[B][1,4]OXAZINE-7-CARBALDEHYDE is a complex chemical compound characterized by a benzoxazine ring with a carbaldehyde group attached, a keto group at the 3-position, and a dihydro functionality at the 3,4-positions. This unique structure and reactivity make it a promising candidate for applications in organic synthesis and pharmaceutical research.
Used in Organic Synthesis:
3-OXO-3,4-DIHYDRO-2H-BENZO[B][1,4]OXAZINE-7-CARBALDEHYDE is used as a building block for the synthesis of more complex organic molecules. Its unique structure allows for the creation of a variety of compounds with different properties and potential applications.
Used in Pharmaceutical Research:
3-OXO-3,4-DIHYDRO-2H-BENZO[B][1,4]OXAZINE-7-CARBALDEHYDE is used as a precursor for the development of new drugs. Its reactivity and unique structure make it a valuable component in the design and synthesis of novel pharmaceutical compounds.
Further research and testing are necessary to fully understand the properties and potential uses of 3-OXO-3,4-DIHYDRO-2H-BENZO[B][1,4]OXAZINE-7-CARBALDEHYDE, as its applications in different industries may vary.

Check Digit Verification of cas no

The CAS Registry Mumber 200195-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,1,9 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 200195-19:
(8*2)+(7*0)+(6*0)+(5*1)+(4*9)+(3*5)+(2*1)+(1*9)=83
83 % 10 = 3
So 200195-19-3 is a valid CAS Registry Number.

200195-19-3SDS

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 3-oxo-4H-1,4-benzoxazine-7-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-oxo-dihydro-2H-benzo[1,4]oxazine-7-carbaldehyde

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:200195-19-3 SDS

200195-19-3Relevant articles and documents

SUBSTITUTED AMINOTHIAZOLES AS INHIBITORS OF NUCLEASES

-

, (2019/11/12)

The invention provides compounds represented by the structural formula (1): wherein R1, R2, R3, R4, R5, R6 are as defined in the claims. The compounds are inhibitors of nucleases, and are useful in particular in a method of treatment and/or prevention of proliferative diseases, neurodegenerative diseases, and other genomic instability associated diseases.

Toward a novel class of antithrombotic compounds with dual function. Discovery of 1,4-benzoxazin-3(4H)-one derivatives possessing thrombin inhibitory and fibrinogen receptor antagonistic activities

Anderluh, Petra ?tefani?,Anderluh, Marko,Ila?, Janez,Mravljak, Janez,Dolenc, Marija Sollner,Stegnar, Mojca,Kikelj, Danijel

, p. 3110 - 3113 (2007/10/03)

A novel class of potential antithrombotic compounds with moderate thrombin inhibitory and fibrinogen receptor antagonistic activity is described. Combination of anticoagulant and antiaggregatory activity in the same molecular entity is presented as a new

Benzoxazinone dopamine D4 receptor antagonists

-

, (2008/06/13)

This invention relates to compounds that are antagonists of dopamine D4 receptors, to methods of treating psychosis and schizophrenia using a compound that is an antagonist of dopamine D4 receptors, and to pharmaceutically acceptable compositions that con

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