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51608-60-7 | (E)-N-Benzylidene-4-methylbenzensulfonamide
CAS No: 51608-60-7 Catalog No: AG003C0X MDL No:
Product Description
Catalog Number:
AG003C0X
Chemical Name:
(E)-N-Benzylidene-4-methylbenzensulfonamide
CAS Number:
51608-60-7
IUPAC Name:
N-benzylidene-4-methylbenzenesulfonamide
InChI:
InChI=1S/C14H13NO2S/c1-12-7-9-14(10-8-12)18(16,17)15-11-13-5-3-2-4-6-13/h2-11H,1H3
InChI Key:
HVCKVBQOKOFBFH-UHFFFAOYSA-N
Properties
Complexity:
369
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
259.067g/mol
Formal Charge:
0
Heavy Atom Count:
18
Hydrogen Bond Acceptor Count:
3
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
259.323g/mol
Monoisotopic Mass:
259.067g/mol
Rotatable Bond Count:
3
Topological Polar Surface Area:
54.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
1
XLogP3:
3.2
Literature
| Title | Journal |
|---|---|
| Green and efficient synthesis of sulfonamides catalyzed by nano-Ru/Fe(3)O(4). | Journal of the American Chemical Society 20090211 |
| Imino ene reaction catalyzed by ytterbium(III) triflate and TMSCl or TMSOTf. | The Journal of organic chemistry 20030418 |
| Asymmetric synthesis of anti- and syn-beta-amino alcohols by reductive cross-coupling of transition metal-coordinated planar chiral arylaldehydes with aldimines. | The Journal of organic chemistry 20021227 |
| Asymmetric synthesis of beta-amino alcohols by reductive cross-coupling of benzylideneamine with planar chiral benzaldehydes. | Organic letters 20020307 |
| Lewis base effects in the Baylis-Hillman reaction of imines with cyclohex-2-en-1-one and cyclopent-2-en-1-one. | Chemical communications (Cambridge, England) 20010921 |
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