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1,4-Dioxaspiro[4.5]deca-6,9-dien-8-one, 2,3-diphenyl-, (2R,3R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

169267-16-7

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169267-16-7 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 22 carbon (C) atoms, 20 hydrogen (H) atoms, and 2 oxygen (O) atoms.
2. Spiro compound

Explanation

A spiro compound is a type of organic compound that contains two rings connected by a shared carbon atom. 1,4-Dioxaspiro[4.5]deca-6,9-dien-8-one, 2,3-diphenyl-, (2R,3R)- has a spiro connection between the dioxaspiro and the diphenyl rings.
3. Aromatic rings

Explanation

The compound contains two aromatic rings, which are characterized by their planar structure and delocalized π-electron systems. Aromatic rings are typically found in many organic compounds and contribute to their stability and reactivity.
4. Cyclic ketal structure

Explanation

A cyclic ketal is a type of acetal formed by the reaction of a ketone with an alcohol, resulting in a cyclic structure. In 1,4-Dioxaspiro[4.5]deca-6,9-dien-8-one, 2,3-diphenyl-, (2R,3R)-, the cyclic ketal structure contributes to its stability and potential reactivity in chemical reactions.
5. Pharmaceutical and medicinal chemistry applications

Explanation

Due to its unique structure and properties, 1,4-Dioxaspiro[4.5]deca-6,9-dien-8-one, 2,3-diphenyl-, (2R,3R)- has potential applications in the development of new pharmaceuticals and as a building block in the synthesis of natural products. Its versatility makes it a valuable compound for research and development in the field of medicinal chemistry.

Explanation

The stereochemistry of a compound refers to the three-dimensional arrangement of its atoms. In this case, the compound has a specific (2R,3R)configuration, which is important for its reactivity and biological activity. This stereochemistry may also make it suitable for use as a chiral ligand or catalyst in chemical reactions.
7. Chiral ligand or catalyst

Explanation

The (2R,3R)configuration of 1,4-Dioxaspiro[4.5]deca-6,9-dien-8-one, 2,3-diphenyl-, (2R,3R)- makes it a potential candidate for use as a chiral ligand or catalyst in chemical reactions. Chiral ligands and catalysts are important in the synthesis of enantiomerically pure compounds, which are often required for pharmaceutical applications.
8. Versatile compound

Explanation

The unique structure and properties of 1,4-Dioxaspiro[4.5]deca-6,9-dien-8-one, 2,3-diphenyl-, (2R,3R)- make it versatile, with diverse potential uses in the fields of chemistry and medicine. Its potential applications in pharmaceutical development, natural product synthesis, and as a chiral ligand or catalyst highlight its versatility and value in research and development.

Stereochemistry

(2R,3R)configuration

Check Digit Verification of cas no

The CAS Registry Mumber 169267-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,2,6 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 169267-16:
(8*1)+(7*6)+(6*9)+(5*2)+(4*6)+(3*7)+(2*1)+(1*6)=167
167 % 10 = 7
So 169267-16-7 is a valid CAS Registry Number.

169267-16-7SDS

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 (2R,3R)-2,3-diphenyl-1,4-dioxaspiro[4.5]deca-6,9-dien-8-one

1.2 Other means of identification

Product number -
Other names 4,4-<(1R,2R)-1,2-(diphenyl)ethylenedioxi>-2,5-cyclohexadienone

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:169267-16-7 SDS

169267-16-7Relevant academic research and scientific papers

Conjugate addition of thiols to p-benzoquinone monoketals. Attempts to prepare chiral synthetic equivalents of p-benzoquinone

De March,Escoda,Figueredo,Font,Mcdrano

, p. 81 - 87 (2007/10/03)

The conjugate addition of several thiols to achiral and chiral p-benzoquinone monoketals has been studied. A chiral synthetic equivalent of p-benzoquinone has been obtained in both enantiopure forms. Springer-Verlag lberica 1997.

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