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7-IODO-1H-BENZO[D][1,3]OXAZINE-2,4-DIONE is a chemical compound characterized by its molecular formula C8H4IN2O3. It is a white crystalline solid known for its unique structure featuring a benzooxazine ring and two carbonyl groups. 7-IODO-1H-BENZO[D][1,3]OXAZINE-2,4-DIONE is primarily utilized as a reagent in chemical reactions and organic synthesis, serving as a building block for the creation of more complex organic molecules. Due to its potential hazards, it is crucial to handle and use 7-IODO-1H-BENZO[D][1,3]OXAZINE-2,4-DIONE with caution, ensuring that only trained professionals work with it in a controlled laboratory environment.

115081-94-2

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115081-94-2 Usage

Uses

Used in Chemical Synthesis:
7-IODO-1H-BENZO[D][1,3]OXAZINE-2,4-DIONE is used as a reagent in chemical reactions for its ability to participate in various organic synthesis processes. Its unique structure with a benzooxazine ring and carbonyl groups makes it a valuable component in the formation of more complex organic molecules.
Used in Research and Development:
In the field of research and development, 7-IODO-1H-BENZO[D][1,3]OXAZINE-2,4-DIONE is employed as a research chemical to explore its properties and potential applications in advancing scientific knowledge and developing new materials or compounds.
Used in Pharmaceutical Industry:
7-IODO-1H-BENZO[D][1,3]OXAZINE-2,4-DIONE is used as an intermediate in the synthesis of pharmaceutical compounds for its potential role in the development of new drugs. Its unique structure may contribute to the creation of novel therapeutic agents.
Used in Material Science:
In material science, 7-IODO-1H-BENZO[D][1,3]OXAZINE-2,4-DIONE is used as a component in the development of new materials, potentially influencing their properties and performance due to its structural characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 115081-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,0,8 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 115081-94:
(8*1)+(7*1)+(6*5)+(5*0)+(4*8)+(3*1)+(2*9)+(1*4)=102
102 % 10 = 2
So 115081-94-2 is a valid CAS Registry Number.

115081-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-iodo-1H-3,1-benzoxazine-2,4-dione

1.2 Other means of identification

Product number -
Other names 4-iodoisatoic 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:115081-94-2 SDS

115081-94-2Relevant academic research and scientific papers

MODIFIED PROTEINS AND PROTEIN DEGRADERS

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Paragraph 001072-001074, (2021/12/08)

Provided herein are compounds, pharmaceutical compositions, and methods for binding or degrading target proteins. Further provided herein are compounds having a DNA damage-binding protein 1 (DDB1) binding moiety. Some such embodiments include a linker. Some such embodiments include a target protein binding moiety. Further provided herein are ligand-DDB1 complexes. Further provided herein are in vivo modified DDB1 proteins.

Synthesis and nematicidal activities of 1,2,3-benzotriazin-4-one containing 4,5-dihydrothiazole-2-thiol derivatives against Meloidogyne incognita

Chen, Xiulei,Zhou, Zhen,Li, Zhong,Xu, Xiaoyong

, p. 194 - 200 (2019/09/13)

A series of novel 1,2,3-benzotriazin-4-one derivatives containing 4,5-dihydrothiazole-2-thiol were synthesized and characterized by 1H NMR, 13C NMR, 19F NMR and HRMS. The bioassay results showed that compounds 3-(3-((4,5-dihydrothiazol-2-yl)thio)propyl)-7-methoxybenzo[d][1–3]triazin-4(3H)-one, 3-(3-((4,5-dihydrothiazol-2-yl)thio)propyl)-6-nitrobenzo[d][1–3]triazin-4(3H)-one, 7-chloro-3-(3-((4,5-dihydrothiazol-2-yl)thio)propyl)benzo[d][1–3]triazin-4(3H)-one exhibited good control efficacy against the cucumber root-knot nematode disease caused by Meloidogyne incognita at the concentration of 10.0 mg L?1 in vivo. Compound 7-chloro-3-(3-((4,5-dihydrothiazol-2-yl)thio)propyl)benzo[d][1–3]triazin-4(3H)-one showed excellent nematicidal activity with inhibition 68.3% at a concentration of 1.0 mg L?1. It suggested that the structure of 1,2,3-benzotriazin-4-one containing 4,5-dihydro-thiazole-2-thiol could be optimized further.

Pyridazinedione compounds useful in treating neurological disorders

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, (2008/06/13)

The present invention relates to pyridazino[4,5-b]quinolines, and pharmaceutically useful salts thereof, which are excitatory amino acid antagonists and which are useful when such antagonism is desired such as in the treatment of neurological disorders. The invention further provides pharmaceutical compositions containing pyridazino[4,5-b]quinolines as active ingredient, and methods for the treatment of neurological disorders.

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