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292-70-6 | 2H-1,2-Oxazocine
CAS No: 292-70-6 Catalog No: AG00BTIH MDL No:
Product Description
Catalog Number:
AG00BTIH
Chemical Name:
2H-1,2-Oxazocine
CAS Number:
292-70-6
IUPAC Name:
2H-oxazocine
InChI:
InChI=1S/C6H7NO/c1-2-4-6-8-7-5-3-1/h1-7H
InChI Key:
RJDZFUUSXRDFCZ-UHFFFAOYSA-N
Properties
Complexity:
56.5
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
109.053g/mol
Formal Charge:
0
Heavy Atom Count:
8
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
109.128g/mol
Monoisotopic Mass:
109.053g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
28.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2
Literature
| Title | Journal |
|---|---|
| Facile synthesis of tetracyclic azepine and oxazocine derivatives and their potential as MAPKAP-K2 (MK2) inhibitors. | Bioorganic & medicinal chemistry letters 20120115 |
| 9-[(2-Hy-droxy-benzyl-idene)amino]-11-(2-hy-droxy-phen-yl)-10,13-diphenyl-8-oxa-12-azoniatricyclo-[7.3.1.0]trideca-2(7),3,5-triene acetate ethanol disolvate. | Acta crystallographica. Section E, Structure reports online 20110301 |
| Amino acid based enantiomerically pure 3-substituted benzofused heterocycles: A new class of antithrombotic agents. | Bioorganic & medicinal chemistry letters 20100101 |
| Diversity-oriented synthetic approach to naturally abundant S-amino acid based benzannulated enantiomerically pure medium ring heterocyclic scaffolds employing inter- and intramolecular mitsunobu reactions. | Journal of combinatorial chemistry 20070101 |
| Design and synthesis of novel 9-substituted-7-aryl-3,4,5,6-tetrahydro-2H-pyrido[4,3-b]- and [2,3-b]-1,5-oxazocin-6-ones as NK(1) antagonists. | Bioorganic & medicinal chemistry letters 20050301 |
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