174563-67-8

Usage

Derivative of 1,3-dioxolane

Yes

Explanation

The compound is derived from 1,3-dioxolane, which is a heterocyclic compound containing two oxygen atoms.

Explanation

The compound contains an acetyl chloride group (-COCl), which is a reactive moiety often used in organic synthesis.

Explanation

The compound has a 2,2-dimethyl-5-oxo group, which is a structural feature that contributes to its chemical properties and reactivity.

Explanation

The compound exists in the (R)-enantiomeric form, which means it has a specific spatial arrangement of atoms that is different from its (S)-enantiomer.

Explanation

It is commonly used as an intermediate in the synthesis of various pharmaceuticals, indicating its importance in the development of new drugs.

Explanation

The compound serves as a reagent for the introduction of acetyl groups and functionalization of molecules, making it a valuable tool in organic chemistry.

Explanation

Due to the presence of the acetyl chloride group and the 2,2-dimethyl-5-oxo moiety, the compound is expected to be highly reactive in various chemical reactions.

Explanation

The (R)-enantiomeric form of the compound indicates that it has chiral centers, which means it can exist in different spatial arrangements that are not mirror images of each other.

Explanation

The compound is likely to be soluble in organic solvents such as dichloromethane, ethyl acetate, or acetone, which is common for compounds with similar structures.

Presence of an acetyl chloride group

Yes

Presence of a 2,2-dimethyl-5-oxo moiety

Yes

(R)-enantiomeric form

Yes

Applications in pharmaceutical synthesis

Yes

Applications in organic chemistry

Yes

Reactivity

High

Stereochemistry

Chiral

Solubility

Soluble in organic solvents