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1-Oxa-7-azaspiro[4.4]non-2-ene-4,6-dione, 8-benzoyl-2-[(2S,4S,5S)-5-(1Z)-1-butenyl-2-methyl-1,3-dioxolan-4-yl]-8, 9-dihydroxy-3-methyl-, (5S,8S,9R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

562858-39-3

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562858-39-3 Usage

Molecular structure

The compound has a complex molecular structure with a spiro[4.4]nonane core, which is a nine-membered ring with a central oxygen atom.

Functional groups

The compound contains various functional groups, such as a benzoyl group (C6H5CO-) and a 1,3-dioxolan-4-yl group.

Carbon, hydrogen, and oxygen content

The compound consists of carbon (C), hydrogen (H), and oxygen (O) atoms, which are essential elements in organic compounds.

Potential applications

Due to its diverse structure and functional groups, the compound may have potential applications in pharmaceuticals, organic synthesis, or other chemical industries.

Need for further research

The properties and uses of this chemical are not yet fully understood, and additional research and analysis are necessary to explore its potential applications and benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 562858-39-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,2,8,5 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 562858-39:
(8*5)+(7*6)+(6*2)+(5*8)+(4*5)+(3*8)+(2*3)+(1*9)=193
193 % 10 = 3
So 562858-39-3 is a valid CAS Registry Number.

562858-39-3Relevant academic research and scientific papers

Asymmetric total synthesis of pseurotin A

Hayashi, Yujiro,Shoji, Mitsuru,Yamaguchi, Shinpei,Mukaiyama, Takasuke,Yamaguchi, Junichiro,Kakeya, Hideaki,Osada, Hiroyuki

, p. 2287 - 2290 (2007/10/03)

(Matrix presented) The asymmetric total syntheses of pseurotin A and 8-O-demethylpseurotin A have been accomplished. Key reactions are a NaH-promoted intramolecular cyclization of an alkynylamide to form a γ-lactam, an aldol reaction of a benzylidene-subs

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