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=1/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: C(O)(=O)[C@]12C(C)(C)[C@](C)(C(=O)O1)CC2

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)-(-)-
• (1R)-(-)-CAMPHANIC ACID
• (1S)-(-)-CAMPHANIC ACID
• (-)-Camphanic acid, (1S)-3-Oxo-4,7,7-trimethyl-2-oxabicyclo[2.2.1]heptane-1-carboxylic acid
• (1S)-(-)-OMEGA-Camphanic acid
• (1S,4R)-3-Oxo-4,7,7-trimethyl-2-oxabicyclo[2.2.1]heptane-1-carboxylic acid
• (1S)-4,7,7-Trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carboxylic acid, (1S)-3-Oxo-4,7,7-trimethyl-2-oxabicyclo[2.2.1]heptane-1-carboxylic acid
• (−
• (1S)-4,7,7-Trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carboxylic acid
• 2-Oxabicyclo2.2.1heptane-1-carboxylic acid, 4,7,7-trimethyl-3-oxo-, (1S,4R)-
• 4,7,7-trimethyl(2-oxabicyclo[2.2.1]hept-1-yl)carboxylic acid
• (IS) CAMPHANIC ACID
• (3R,6S)-2-Oxo-3β,6β-isopropylidene-3-methyltetrahydro-2H-pyran-6-carboxylic acid
• (-)-CAMPHANIC ACID 98+%
• 1,7,7-Trimethyl-2-oxo-3-oxabicyclo[2.2.1]heptane-4-carboxylic acid
• (1S)-3-OXO-4,7,7-TRIMETHYL-2-OXABICYCLO[2.2.1]HEPTANE-1-CARBOXYLIC ACID

(-)-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

Ref: 3B-C1021

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

CAS: 13429-83-9

Formula: C₁₀H₁₄O₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 198.2158

Ref: IN-DA003AY5

(-)-Camphanic acid

CAS: 13429-83-9

(-)-Camphanic acid

Purity: 98%

Molecular weight: 198.22g/mol

Ref: 54-OR5941

(-)-Camphanic acid

CAS: 13429-83-9

Formula: C₁₀H₁₄O₄

Molecular weight: 198.22

Ref: 7W-GK1298

(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

Ref: 3D-FC46445

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

CAS: 13429-83-9

Formula: C₁₀H₁₄O₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 198.218

Ref: 10-F435870

(S)-Camphanic Acid

Controlled Product

CAS: 13429-83-9

Applications (S)-Camphanic Acid is used in the enantiomer separation of useful chiral building blocks.
References Bieliunas, V., et al.: J. Org. Chem., 78, 5339 (2013);

Formula: C₁₀H₁₄O₄

Color and Shape: Neat

Molecular weight: 198.22

Ref: TR-C175110