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Catalog Number:
39163
CAS Number:
40724-67-2
(S)-(+)-Ketopinic acid
Purity:
≥ 98% (Assay by titration , GC)
Synonym(s):
(1S)-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptane-1-carboxylicacid
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Product Information

(S)-(+)-Ketopinic acid is a chiral bicyclic compound that has garnered attention in various fields, particularly in pharmaceuticals and organic synthesis. This compound is recognized for its unique structural properties, which make it a valuable intermediate in the synthesis of various bioactive molecules. Its ability to act as a chiral building block allows researchers to create compounds with specific stereochemistry, essential for developing effective drugs.

In the pharmaceutical industry, (S)-(+)-Ketopinic acid is utilized in the synthesis of compounds that exhibit significant biological activity, including potential applications in treating neurological disorders. Its distinctive bicyclic structure provides advantages in terms of stability and reactivity compared to other similar compounds, making it a preferred choice for researchers looking to optimize their synthetic pathways. With its growing relevance in medicinal chemistry and organic synthesis, (S)-(+)-Ketopinic acid stands out as a compound with promising applications and benefits for industry professionals.

Synonyms
(1S)-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptane-1-carboxylicacid
CAS Number
40724-67-2
Purity
≥ 98% (Assay by titration , GC)
Molecular Formula
C10H14O3
Molecular Weight
182.22
MDL Number
MFCD00168053
PubChem ID
297888
Melting Point
235 - 240 °C
Appearance
White to off-white crystalline powder
Optical Rotation
[α]20D = 25.5 ° (C = 0.65 in MeOH)
Conditions
Store at RT
General Information
Synonyms
(1S)-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptane-1-carboxylicacid
CAS Number
40724-67-2
Purity
≥ 98% (Assay by titration , GC)
Molecular Formula
C10H14O3
Molecular Weight
182.22
MDL Number
MFCD00168053
PubChem ID
297888
Melting Point
235 - 240 °C
Appearance
White to off-white crystalline powder
Optical Rotation
[α]20D = 25.5 ° (C = 0.65 in MeOH)
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-(+)-Ketopinic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important building block in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Chiral Synthesis: Its chiral nature makes it valuable in asymmetric synthesis, allowing chemists to create enantiomerically pure compounds, which are crucial for the efficacy and safety of many medications.
  • Biochemical Research: Researchers use (S)-(+)-Ketopinic acid to study metabolic pathways and enzyme interactions, enhancing our understanding of biological processes.
  • Material Science: This compound is explored for its potential applications in creating new materials with specific properties, such as polymers that can be used in drug delivery systems.
  • Analytical Chemistry: It is employed as a standard in analytical methods to ensure accurate measurements and quality control in various chemical analyses.

Citations