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58042-39-0 | N-Hydroxy-2,4,6-trimethylbenzenesulfonamide
CAS No: 58042-39-0 Catalog No: AG003T2C MDL No:MFCD16309113
Product Description
Catalog Number:
AG003T2C
Chemical Name:
N-Hydroxy-2,4,6-trimethylbenzenesulfonamide
CAS Number:
58042-39-0
Molecular Formula:
C9H13NO3S
Molecular Weight:
215.2694
MDL Number:
MFCD16309113
IUPAC Name:
N-hydroxy-2,4,6-trimethylbenzenesulfonamide
InChI:
InChI=1S/C9H13NO3S/c1-6-4-7(2)9(8(3)5-6)14(12,13)10-11/h4-5,10-11H,1-3H3
InChI Key:
RRPKGUUYTHFUPN-UHFFFAOYSA-N
SMILES:
ONS(=O)(=O)c1c(C)cc(cc1C)C
Properties
Complexity:
271
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
215.062g/mol
Formal Charge:
0
Heavy Atom Count:
14
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
215.267g/mol
Monoisotopic Mass:
215.062g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
74.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.5
Literature
| Title | Journal |
|---|---|
| Facile conversion of cysteine and alkyl cysteines to dehydroalanine on protein surfaces: versatile and switchable access to functionalized proteins. | Journal of the American Chemical Society 20080416 |
| Mild preparation of alkenes from phenyl sulfides: one-pot elimination of phenylthio group via sulfilimine at ambient temperature. | Organic letters 20061221 |
| Synthesis and palladium-catalyzed coupling reactions of enantiopure p-bromophenyl methyl sulfoximine. | The Journal of organic chemistry 20050318 |
| [How have we found any new reactions in the field of the heterocyclic chemistry?]. | Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 20040401 |
| Highly efficient synthesis of O-(2,4-dinitrophenyl)hydroxylamine. Application to the synthesis of substituted N-benzoyliminopyridinium ylides. | The Journal of organic chemistry 20030905 |
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