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1,4-Dioxa-2-azaspiro[4.5]dec-2-ene, 3-phenyl- is a complex organic compound characterized by a unique spirocycle structure. The molecule features a seven-membered ring with a nitrogen atom and two oxygen atoms, forming a spiro connection with a five-membered ring. The phenyl group is attached to the third carbon of the seven-membered ring, which imparts additional stability and aromatic character to the molecule. 1,4-Dioxa-2-azaspiro[4.5]dec-2-ene, 3-phenyl- is of interest in organic chemistry due to its potential applications in the synthesis of pharmaceuticals and other specialty chemicals, as well as its intriguing molecular architecture that can be further functionalized or studied for its physical and chemical properties.

2290-00-8

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2290-00-8 Usage

Chemical class

Spiro compounds

Explanation

1,4-Dioxa-2-azaspiro[4.5]dec-2-ene, 3-phenylbelongs to the group of spiro compounds, which are characterized by a spirocyclic structure.

Explanation

The compound has a spirocyclic structure, which means it consists of two rings connected by a shared carbon atom. In this case, the structure includes two oxygen atoms and one nitrogen atom.

Explanation

The "3-phenyl-" part of the compound indicates the presence of a phenyl group, which is a six-carbon aromatic ring with a hydrogen atom attached, at the 3rd position of the spirocyclic structure.

Explanation

Due to its unique structure, 1,4-Dioxa-2-azaspiro[4.5]dec-2-ene, 3-phenylmay have potential applications in the pharmaceutical industry or in organic synthesis. However, further research is needed to confirm these applications.

Explanation

The structure of the compound suggests that it may have potential biological activity, which could be useful in the development of new drugs or other biologically active molecules. However, this should be verified through scientific research and experimentation.

Explanation

The specific properties and uses of 1,4-Dioxa-2-azaspiro[4.5]dec-2-ene, 3-phenylshould be further investigated and verified through scientific research and experimentation to fully understand its potential applications and limitations.

Structure

Spirocycle with two oxygen atoms and one nitrogen atom

Substituent

3-phenyl

Potential applications

Pharmaceutical industry and organic synthesis

Biological activity

Possible

Further investigation

Required

Check Digit Verification of cas no

The CAS Registry Mumber 2290-00-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,9 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2290-00:
(6*2)+(5*2)+(4*9)+(3*0)+(2*0)+(1*0)=58
58 % 10 = 8
So 2290-00-8 is a valid CAS Registry Number.

2290-00-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl-1,4-dioxa-2-aza-spiro[4.5]dec-2-ene

1.2 Other means of identification

Product number -
Other names 3-Phenyl-1,4,2-dioxazolin-5-spirocyclohexan

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:2290-00-8 SDS

2290-00-8Downstream Products

2290-00-8Relevant academic research and scientific papers

Synthesis of five-membered cyclic nitrones based on the Lewis acid-catalysed [3+2]-annulation reaction of donor-acceptor cyclopropanes with 1,4,2-dioxazoles

Wang, Zhe-Hao,Zhang, Huan-Huan,Xu, Peng-Fei,Luo, Yong-Chun

, p. 10128 - 10131 (2018)

A novel synthesis of five-membered cyclic nitrones has been developed based on the Lewis acid-catalysed [3+2]-annulation reaction of D-A cyclopropanes with 1,4,2-dioxazoles. Broad substrate scope and generally good yield make this reaction useful in the p

The photochemistry of acyl azides - IX. Direct and sensitized photolytic generation of acylnitrenes for cycloaddition reactions

Clauss, Kai-Uwe,Buck, Karin,Abraham, Werner

, p. 7181 - 7192 (2007/10/02)

Contrary to ethoxycarbonylnitrene, selective reactions - including cycloadditions - can be carried out with benzoylnitrene. This study analyzes the sequence of reactivity of various bond types with respect to benzoylnitrene, which was generated by three different routes: direct photolysis of benzoyl azide, sensitization of azide decomposition via energy transfer, and photoinduced electron transfer. In all cases the same cycloadducts 23, 24, and 30 were obtained. Carbonyl activity determines the reactivity of unsaturated ketones and aldehydes with respect to benzoylnitrene.

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