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(R,S)-Camphorsulfonic acid Isopropyl Ester

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For Research Use Only | Not For Clinical Use
CATAPB1242184402
CAS1242184-40-2
Synonymsisopropyl ((1R,4S)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonate
Molecular Weight274.38
Molecular FormulaC13H22O4S

What is the product name of CAS 1242184-40-2?

The product name is (R,S)-Camphorsulfonic acid Isopropyl Ester.

What is the chemical formula of (R,S)-Camphorsulfonic acid Isopropyl Ester?

The chemical formula is C13H22O4S.

What is the molecular weight of (R,S)-Camphorsulfonic acid Isopropyl Ester?

The molecular weight is 274.38.

What are the synonyms of (R,S)-Camphorsulfonic acid Isopropyl Ester?

One of the synonyms is isopropyl ((1R,4S)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonate.

What is the CAS number of (R,S)-Camphorsulfonic acid Isopropyl Ester?

The CAS number is 1242184-40-2.

What is the structure of the (R,S)-Camphorsulfonic acid Isopropyl Ester molecule?

The structure contains a bicyclic ring system with a sulfonic acid group attached to an isopropyl ester.

How is (R,S)-Camphorsulfonic acid Isopropyl Ester commonly used in the industry?

It is commonly used as a reagent or catalyst in organic synthesis.

What is the significance of the stereochemistry designated by (R,S) in the name?

It indicates the chirality of the molecule, which is important in determining its specific optical properties.

What is the role of the isopropyl ester group in (R,S)-Camphorsulfonic acid Isopropyl Ester?

The isopropyl ester group serves as a protecting group for the sulfonic acid functionality.

How does (R,S)-Camphorsulfonic acid Isopropyl Ester contribute to the overall stereochemistry of a reaction?

It can influence the stereochemistry of a reaction through its chiral center, leading to selective product formation in certain reactions.

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