CAS 32508-22-8

2-Methylbicyclo[2.2.1]heptane-2-carboxylic acid

Description:

2-Methylbicyclo[2.2.1]heptane-2-carboxylic acid, with the CAS number 32508-22-8, is a bicyclic organic compound characterized by its unique bicyclic structure, which consists of a seven-membered ring system. This compound features a carboxylic acid functional group (-COOH) attached to the second carbon of the bicyclic framework, along with a methyl group (-CH3) at the same position, contributing to its overall stability and reactivity. The presence of the carboxylic acid group imparts acidic properties, allowing it to participate in various chemical reactions, such as esterification and decarboxylation. The compound is typically colorless to pale yellow in appearance and is soluble in polar solvents due to the hydrophilic nature of the carboxylic acid group. Its structural characteristics make it of interest in organic synthesis and potential applications in pharmaceuticals or agrochemicals. As with many organic compounds, handling should be done with care, considering safety protocols to avoid exposure or adverse reactions.

Formula: C₉H₁₄O₂

InChI: InChI=1/C9H14O2/c1-9(8(10)11)5-6-2-3-7(9)4-6/h6-7H,2-5H2,1H3,(H,10,11)

InChI key: InChIKey=JZKREHRYLBOJRP-UHFFFAOYSA-N

SMILES: C(O)(=O)C1(C)C2CC(C1)CC2

Synonyms:

• 2-Norbornanecarboxylic acid, 2-methyl-
• Bicyclo(2.2.1)heptane-2-carboxylic acid, 2-methyl-
• 2-Methylbicyclo(2.2.1)heptane-2-carboxylic acid
• 2-Methylbicyclo[2.2.1]heptane-2-carboxylic acid
• BCHC
• 2-Methylbicylo-(2,2,1)-Heptane-2-Carboxylic

2-Methylbicyclo[2.2.1]heptane-2-carboxylic acid

CAS: 32508-22-8

2-Methylbicyclo[2.2.1]heptane-2-carboxylic acid is a carotenoid that is found in some bacteria and plants, including the green alga Chlorella sorokiniana. It has been shown to have anticancer activity by inducing apoptosis in cancer cells. 2-Methylbicyclo[2.2.1]heptane-2-carboxylic acid also reduces the redox potential of cancer cells and inhibits their growth, which may be due to its ability to regulate cell cycle progression and inhibit protein synthesis. This compound also has been shown to stimulate the formation of bacteriochlorophyll a and membrane systems in bacteria, such as Escherichia coli and Pseudomonas aeruginosa, respectively. The gene product responsible for this carotenoid biosynthesis has been identified as a transcriptional regulator of dna binding activity and protein expression in Escher

Formula: C₉H₁₄O₂

Purity: Min. 95%

Molecular weight: 154.21 g/mol

Ref: 3D-HBA50822