(1S)-(+)-10-Camphorsulfonic acid

CAS: 3144-16-9

Ref. 3D-FC19651

Product Information

• Name: (1S)-(+)-10-Camphorsulfonic acid
• Synonyms: (1S,4R)-7,7-Dimethyl-2-oxo-bicyclo[2.2.1]heptane-1-methanesulfonic acid(+)-Camphor-10-sulfonic acid(+)-b-Camphorsulfonic acid, ((1S,4R)-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonic acid, (+)-(S)-Camphor-10-sulfonic acid, (+)-2-Oxo-10-bornanesulfonic acid, (+)-<span class="text-smallcaps">D</span>-Camphor-10-sulfonic acid, (+)-Camphor-10-Sulfonicacid (Beta), (+)-Camphor-10-Sulphonic Acid, (+)-Camphor-10-sulfonic acid, (+)-Camphor-ω-sulfonic acid, (+)-Β-Camphorsulfonic Acid, (1S)-camphor-10-sulfonic acid, (1S,4R)-10-Camphorsulfonic acid, (1S,4R)-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulfonic acid, (S)-(+)-Csa, (S)-Camphorsulfonic acid, 10-Bornanesulfonic acid, 2-oxo-, (1S,4R)-(+)-, 2-Oxobornan-10-sulfonsaure, 2-Oxobornane-10-Sulphonic Acid, <span class="text-smallcaps">D</span>-(+)-Camphorsulfonic acid, <span class="text-smallcaps">D</span>-Camphor-β-sulfonic acid, Acide 2-oxobornane-10-sulfonique, Acido 2-Oxobornano-10-Sulfonico, Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-, Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S,4R)-, D(-)-Camphorsulfonic acid, D-(+)-Camphor Sulfonic Acid, D-(+)-Camphor-10-Sulfonic Acid, D-(+)-camphour sulphonic acid, D-2-Oxobornane-10-Sulfonic Acid, D-Camphor-β-sulfonic acid, L-(-)-Camphor-10-sulfonic acid monohydrate, Reychler's acid, S(+)Camphor sulfonic acid, [(1R)-7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl]methanesulfonic acid, [(1R,4R)-7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl]methanesulfonate, [(1S)-7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl]methanesulfonic acid, [(1S,4R)-7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl]methanesulfonic acid, [(1S,4S)-7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl]methanesulfonate, d-10-Camphorsulfonic acid

Description

(1S)-(+)-10-Camphorsulfonic acid is an organolithium compound that is used as a reagent in organic synthesis. It has been shown to have antimicrobial activity against Gram-positive and Gram-negative bacteria, including methicillin-resistant Staphylococcus aureus (MRSA). The bathochromic shift observed in the infrared spectrum of camphorsulfonic acid at 860 nm is due to the hydrogen bonding between sulfonic acid groups. Camphorsulfonic acid has also been shown to inhibit dipeptidyl peptidase-IV, which results in increased levels of butyric acid, a short chain fatty acid. This inhibition may be responsible for its use as an adjuvant for vaccines.

• Brand: Biosynth

Chemical properties

• Molecular weight: 232.3 g/mol
• Formula: C₁₀H₁₆O₄S
• Purity: Min. 95%
• Color/Form: Powder