(1R)-10-Camphorsulfonamide

C10H17NO3SCAS 72597-34-3231.31 g/mol

Open in Covalent MOL file
SNH2OOO
KetoneSulfonamide

Properties

Molecular formula
C10H17NO3S
Molar mass
231.31 g/mol
Exact mass
231.0929 Da
logP
0.67Crippen estimate
Polar surface area
77.2 Ų
H-bond donors / acceptors
1 / 3
Rotatable bonds
2
Stereocentres
S, Rin SMILES atom order

Hazards

No GHS classification is on file for this compound. That is not evidence that it is harmless.

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Identifiers

CAS number
72597-34-3
SMILES
CC1(C)[C@H]2CC[C@]1(CS(N)(=O)=O)C(=O)C2
InChIKey
SBLUNABTQYDFJM-XVKPBYJWSA-N
InChI
InChI=1S/C10H17NO3S/c1-9(2)7-3-4-10(9,8(12)5-7)6-15(11,13)14/h7H,3-6H2,1-2H3,(H2,11,13,14)/t7-,10-/m0/s1

Weigh it out

Type any one amount. The others follow from the molar mass.

Names and synonyms

6 names
  • Bicyclo[2.2.1]heptane-1-methanesulfonamide, 7,7-dimethyl-2-oxo-, (1R,4S)-
  • Bicyclo[2.2.1]heptane-1-methanesulfonamide, 7,7-dimethyl-2-oxo-, (1R)-
  • d-10-Camphorsulfonamide
  • (1R,4S)-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulfonamide
  • [[((1R,4S)-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methyl]sulfonyl]amine
  • ((1R,4S)-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonamide

Work with (1R)-10-Camphorsulfonamide

Predict the NMR spectrum1H and 13C shifts with multiplicities Make a solutionWhat to weigh for any molarity and volume Check drug-likenessLipinski, Veber and lead-likeness Isotope patternExact mass and the mass spectrum pattern

Stereoisomers, salts and isotopologues

The same compound in another form: other stereochemistry, a salt or hydrate, the free acid or base, or an isotope-labelled version.

(1S)-(+)-10-Camphorsulfonamide60933-63-3Stereoisomer

Similar compounds

Camphor-10-sulfonyl chloride21286-54-466 % similar Camphorsulfonic acid3144-16-966 % similar (-)-Camphorsulfonic acid35963-20-366 % similar Camphorsulfonic acid5872-08-266 % similar Sodium (+)-10-camphorsulfonate21791-94-661 % similar Sodium dl-10-camphorsulfonate34850-66-361 % similar (±)-Camphor21368-68-348 % similar (-)-Camphor464-48-248 % similar

Tanimoto similarity of circular fingerprints over the whole catalogue.

All similar compounds

Elsewhere

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