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Home > Indoles and Oxindole > 31271-90-6
31271-90-6 | N-(P-TOLUENESULFONYL)INDOLE
CAS No: 31271-90-6 Catalog No: AG003SF7 MDL No:
Product Description
Catalog Number:
AG003SF7
Chemical Name:
N-(P-TOLUENESULFONYL)INDOLE
CAS Number:
31271-90-6
IUPAC Name:
1-(4-methylphenyl)sulfonylindole
InChI:
InChI=1S/C15H13NO2S/c1-12-6-8-14(9-7-12)19(17,18)16-11-10-13-4-2-3-5-15(13)16/h2-11H,1H3
InChI Key:
JNRRPYFLDADLJW-UHFFFAOYSA-N
Properties
Complexity:
406
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
271.067g/mol
Formal Charge:
0
Heavy Atom Count:
19
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
271.334g/mol
Monoisotopic Mass:
271.067g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
47.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.6
Literature
| Title | Journal |
|---|---|
| The benzyne Fischer-indole reaction. | Organic letters 20110715 |
| Anti HIV-1 agents 5: synthesis and anti-HIV-1 activity of some N-arylsulfonyl-3-acetylindoles in vitro. | Bioorganic & medicinal chemistry letters 20100615 |
| Direct cyanation of heteroaromatic compounds mediated by hypervalent iodine(III) reagents: In situ generation of PhI(III)-CN species and their cyano transfer. | The Journal of organic chemistry 20070105 |
| Oligomerization of N-tosylindole with aluminum chloride. | Bioscience, biotechnology, and biochemistry 20040301 |
| Development of an indole safety-catch linker using analytical constructs. | Journal of combinatorial chemistry 20040101 |
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