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(1S)-(+)-Camphor-10-sulfonic acid(dry wt.),water

Catalog Number
ACM3144169-1
Product Name
(1S)-(+)-Camphor-10-sulfonic acid(dry wt.),water
Structure
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CAS
3144-16-9
  • Product Overview
  • Usage
Synonyms
(1S)-(+)-10-Camphorsulfonic acid, 99%; Camphersulfosaeure [German]; ST2408078; DL-10-Camphorsulfonic acid; CS-D1796; [(1S,4R)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl]methanesulfonic acid; Voriconazole Impurity E; D-Camphor sulfonic acid, United States Pharmacopeia (USP) Reference Standard; MFCD00074827; Camphor-10-sulfonic acid (beta), 98%;
IUPAC Name
[(1S,4R)-7,7-dimethyl-2-oxo-1-bicyclo[2.2.1]heptanyl]methanesulfonic acid;
Molecular Weight
232.294g/mol
Molecular Formula
C10H16O4S;
Canonical SMILES
CC1(C2CCC1(C(=O)C2)CS(=O)(=O)O)C;
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;
Storage
2-8°C
Complexity
404
Covalently-Bonded Unit Count
1
Defined Atom Stereocenter Count
2
EC Number
221-554-1
Exact Mass
232.077g/mol
H-Bond Acceptor
4
H-Bond Donor
1
Heavy Atom Count
15
Monoisotopic Mass
232.077g/mol
NSC Number
4167
Rotatable Bond Count
2
Topological Polar Surface Area
79.8A^2
UNII
9TLZ01S15L
Application
The purpose of (1S)-(+)-Camphor-10-sulfonic acid, which appears as a white to light beige powder, is to serve as a highly effective resolving agent and a catalyst for coupling dipeptides. It acts as a stabilizer in various chemical processes, showcasing its versatility. In particular, this compound is instrumental in the synthesis of chiral polyaniline (PANI) nanofibers through an efficient potentiostatic electropolymerization method conducted without a template, utilizing (1S)-(+)-camphor-10-sulfonic acid (D-CSA) or its enantiomer, (1R)-(-)camphor-10-sulfonic acid (L-CSA), as a dopant. Additionally, it plays a key role in the production of quaternary ammonium compounds (QUATs) derived from its structure, underscoring its importance in advanced material synthesis and catalysis.
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