Home Aminos (6-amino-3,4-dihydro-2H-1,4-benzoxazin-3-yl)methanol

(6-amino-3,4-dihydro-2H-1,4-benzoxazin-3-yl)methanol

CAS No.:
896126-03-7
Catalog Number:
AG01B1NN
Molecular Formula:
C9H12N2O2
Molecular Weight:
180.2038
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Product Description
Catalog Number:
AG01B1NN
Chemical Name:
(6-amino-3,4-dihydro-2H-1,4-benzoxazin-3-yl)methanol
CAS Number:
896126-03-7
Molecular Formula:
C9H12N2O2
Molecular Weight:
180.2038
MDL Number:
MFCD20668331
IUPAC Name:
(6-amino-3,4-dihydro-2H-1,4-benzoxazin-3-yl)methanol
InChI:
InChI=1S/C9H12N2O2/c10-6-1-2-9-8(3-6)11-7(4-12)5-13-9/h1-3,7,11-12H,4-5,10H2
InChI Key:
QULMQWMDJWXOMS-UHFFFAOYSA-N
SMILES:
Nc1cc2NC(CO)COc2cc1
Properties
Complexity:
177  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
180.09g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
180.207g/mol
Monoisotopic Mass:
180.09g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
67.5A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
0.4  
Literature
Title Journal
Role of Hmbox1 in endothelial differentiation of bone-marrow stromal cells by a small molecule. ACS chemical biology 20101119
Distinct patterns of autophagy evoked by two benzoxazine derivatives in vascular endothelial cells. Autophagy 20101101
Discovery of a benzoxazine derivative promoting angiogenesis in vitro and in vivo. Journal of cellular physiology 20100401
Protective effects of a benzoxazine derivative against oxidized LDL-induced apoptosis and the increases of integrin beta4, ROS, NF-kappaB and P53 in human umbilical vein endothelial cells. Bioorganic & medicinal chemistry letters 20090515
Design, synthesis, and preliminary biological evaluation of 2,3-dihydro-3-hydroxymethyl-1,4-benzoxazine derivatives. Bioorganic & medicinal chemistry letters 20060601
Properties