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

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

CAS No.:
3144-16-9
Catalog Number:
AG003BCF
Molecular Formula:
C10H16O4S
Molecular Weight:
232.2966
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$19
- +
100g
98%
In Stock USA
United States
$50
- +
500g
98%
In Stock USA
United States
$188
- +
Product Description
Catalog Number:
AG003BCF
Chemical Name:
(1S)-(+)-10-Camphorsulfonic acid
CAS Number:
3144-16-9
Molecular Formula:
C10H16O4S
Molecular Weight:
232.2966
MDL Number:
MFCD00150752
IUPAC Name:
[(1S,4R)-7,7-dimethyl-2-oxo-1-bicyclo[2.2.1]heptanyl]methanesulfonic acid
InChI:
InChI=1S/C10H16O4S/c1-9(2)7-3-4-10(9,8(11)5-7)6-15(12,13)14/h7H,3-6H2,1-2H3,(H,12,13,14)/t7-,10-/m1/s1
InChI Key:
MIOPJNTWMNEORI-GMSGAONNSA-N
SMILES:
O=C1C[C@@H]2C([C@]1(CC2)CS(=O)(=O)O)(C)C
UNII:
9TLZ01S15L
NSC Number:
4167
Properties
Complexity:
404  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Defined Bond Stereocenter Count:
0
Exact Mass:
232.077g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
232.294g/mol
Monoisotopic Mass:
232.077g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
79.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.5  
Literature
Title Journal
Camphorsulfonic acid catalysed facile tandem double Friedlander annulation protocol for the synthesis of phenoxy linked bisquinoline derivatives and discovery of antitubercular agents. Bioorganic & medicinal chemistry letters 20120215
Primary amine/CSA ion pair: a powerful catalytic system for the asymmetric enamine catalysis. Organic letters 20110520
Determination of bile acids in pig liver, pig kidney and bovine liver by gas chromatography-chemical ionization tandem mass spectrometry with total ion chromatograms and extraction ion chromatograms. Journal of chromatography. A 20110121
Analysis of deprotonated acids with silicon nanoparticle-assisted laser desorption/ ionization mass spectrometry. Journal of mass spectrometry : JMS 20101201
Design and construction of a compact end-station at NSRRC for circular-dichroism spectra in the vacuum-ultraviolet region. Journal of synchrotron radiation 20101101
Primary amine/(+)-CSA salt-promoted organocatalytic conjugate addition of nitro esters to enones. Organic letters 20100521
Swift heavy ion irradiation induced enhancement in the antioxidant activity and biocompatibility of polyaniline nanofibers. Nanotechnology 20100430
(S)-Camphorsulfonic acid catalyzed highly stereoselective synthesis of pseudoglycosides. Bioorganic & medicinal chemistry letters 20090601
Solute-solvent interactions in imidazolium camphorsulfonate ionic liquids. Physical chemistry chemical physics : PCCP 20071128
Micellar peroxidase-catalyzed synthesis of chiral polyaniline. Biomacromolecules 20070801
Effect of (+) or (-) camphorsulfonic acid additives to the mobile phase on enantioseparations of some basic drugs on a Chiralcel OD column. Journal of chromatography. A 20050812
Redetermination of the extinction coefficient of camphor-10-sulfonic acid, a calibration standard for circular dichroism spectroscopy. Analytical biochemistry 20041215
Enantiomeric separation of basic compounds using heptakis(2,3-di-O-methyl-6-O-sulfo)-beta-cyclodextrin in combination with potassium camphorsulfonate in nonaqueous capillary electrophoresis: optimization by means of an experimental design. Electrophoresis 20040801
Transglucosidation of methyl and ethyl D-glucopyranosides by alcoholysis. Carbohydrate research 20020315
Properties