CAS 13429-83-9: (1S)-(-)-Camphanic acid

Description: (1S)-(-)-Camphanic acid is a bicyclic organic compound derived from camphor, characterized by its unique structure that includes a cyclobutane ring fused to a cyclopentane ring. It is a chiral molecule, exhibiting optical activity due to the presence of a single stereocenter, which contributes to its specific rotation. This compound is typically a white crystalline solid with a melting point that can vary based on purity and environmental conditions. (1S)-(-)-Camphanic acid is known for its distinctive odor and is often used in the synthesis of various pharmaceuticals and fragrances. It can participate in various chemical reactions, including esterification and amidation, making it valuable in organic synthesis. Additionally, it has applications in the field of asymmetric synthesis due to its chiral nature. The compound is soluble in organic solvents but has limited solubility in water, which is common for many organic acids. Safety data should be consulted for handling and storage, as with any chemical substance.

Formula: C₁₀H₁₄O₄

InChI: InChI=1S/C10H14O4/c1-8(2)9(3)4-5-10(8,6(11)12)14-7(9)13/h4-5H2,1-3H3,(H,11,12)/t9-,10+/m0/s1

InChI key: InChIKey=KPWKPGFLZGMMFX-VHSXEESVSA-N

SMILES: O=C(O)C12OC(=O)C(C)(CC1)C2(C)C

Synonyms:

• (-)-Camphanic acid
• (-)-ω-Camphanic acid
• (1R)-4,7,7-trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carboxylic acid
• (1R,4R)-4,7,7-Trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carboxylic acid
• (1R,4S)-4,7,7-trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carboxylate
• (1S,4R)-(-)-Camphanic acid
• (1S,4R)-4,7,7-trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carboxylate
• (1S,4R)-4,7,7-trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carboxylic acid
• (1S,4R)-ω-Camphanic acid
• (S)-Camphanic acid
• 2-Oxabicyclo[2.2.1]heptane-1-carboxylic acid, 4,7,7-trimethyl-3-oxo-, (1S)-
• 2-Oxabicyclo[2.2.1]heptane-1-carboxylic acid, 4,7,7-trimethyl-3-oxo-, (1S,4R)-
• 3-(2-Methoxyphenoxy)Propane-1,2-Diol
• 4,7,7-Trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carboxylic acid
• Camphanic acid, (1S)-(-)-

(-)-Camphanic Acid

CAS: 13429-83-9

• Formula: C₁₀H₁₄O₄
• Purity: >98.0%(T)
• Color and Shape: White to Almost white powder to crystaline
• Molecular weight: 198.22

(1S)-4,7,7-Trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carboxylic acid

CAS: 13429-83-9

• Formula: C₁₀H₁₄O₄
• Purity: 96%
• Color and Shape: Solid
• Molecular weight: 198.2158

(-)-Camphanic acid

CAS: 13429-83-9

• Purity: 98+%
• Molecular weight: 198.22g/mol

(-)-Camphanic acid

CAS: 13429-83-9

• Formula: C₁₀H₁₄O₄
• Molecular weight: 198.22

(1S)-4,7,7-Trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carboxylic acid

CAS: 13429-83-9

• Purity: 98.0%
• Color and Shape: Solid
• Molecular weight: 198.21800231933594

(1S)-(-)-Camphanic acid

CAS: 13429-83-9

A chiral auxiliary for the separation of racemates

• Formula: C₁₀H₁₄O₄
• Purity: Min. 95%
• Color and Shape: White Powder
• Molecular weight: 198.22 g/mol

(S)-Camphanic Acid

CAS: 13429-83-9

Applications (S)-Camphanic Acid is used in the enantiomer separation of useful chiral building blocks. References …

• Formula: C₁₀H₁₄O₄
• Color and Shape: Neat
• Molecular weight: 198.22