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1,3-Dioxolane-4-carboxaldehyde, 2-ethyl-2-methyl-, (4R)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

500021-09-0

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500021-09-0 Usage

Explanation

This is the commonly used name for the compound, which helps in identifying it easily among chemists and researchers.

Explanation

The chemical structure describes the arrangement of atoms in the molecule, which determines its properties and reactivity.

Explanation

The (4R)notation indicates the specific configuration of the molecule, which is important for its stereochemistry and potential biological activity.

Explanation

The compound is a liquid at room temperature, which is important for its handling and use in chemical reactions.

Explanation

The compound has a pleasant, fruity odor, which can be useful for identifying it in the lab or for its use in the fragrance industry.

Explanation

The compound is known for its reactivity, making it a valuable building block in organic synthesis.

Explanation

Due to its reactivity and unique structure, the compound is used as an intermediate in the production of various pharmaceuticals and organic compounds.

Explanation

The compound should be handled with care due to its potential to cause skin and eye irritation. Additionally, it is flammable, which requires proper safety measures during storage and use.

Explanation

The chemical properties and reactivity of 1,3-Dioxolane-4-carboxaldehyde, 2-ethyl-2-methyl-, (4R)(9CI) make it a valuable tool for researchers and chemists working in the field of organic chemistry.

Chemical Structure

1,3-Dioxolane ring with a carbaldehyde group at the 4-position, an ethyl group at the 2-position, and a methyl group at the 2-position.

Optical Isomer

(4R)-

Physical State

Colorless liquid

Odor

Fruity

Reactivity

Highly reactive

Applications

Intermediate in the synthesis of pharmaceuticals and other organic compounds

Safety Precautions

Potential for skin and eye irritation, flammability

Importance in Organic Chemistry

Useful tool in the field of organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 500021-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,0,2 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 500021-09:
(8*5)+(7*0)+(6*0)+(5*0)+(4*2)+(3*1)+(2*0)+(1*9)=60
60 % 10 = 0
So 500021-09-0 is a valid CAS Registry Number.

500021-09-0Upstream product

500021-09-0Relevant articles and documents

Trifluoroacetic anhydride promoted tandem conjugate addition of boronic acids/acetal ring opening

Roscales, Silvia,Csaky, Aurelio G.

supporting information; experimental part, p. 1187 - 1189 (2012/04/17)

A new stereoselective tandem reaction consisting of the metal-free conjugate addition of boronic acids followed by an intramolecular ring opening of a cyclic acetal has been disclosed. Optically pure polysubstituted tetrahydropyrans have been synthesized

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