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Home Other Building Blocks 2-Methoxybenzamide

2-Methoxybenzamide

CAS No.:
2439-77-2
Catalog Number:
AG003HJQ
Molecular Formula:
C8H9NO2
Molecular Weight:
151.1626
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
99%(GC)
In Stock USA
United States
$121
- +
10g
99%(GC)
In Stock USA
United States
$211
- +
25g
99%(GC)
In Stock USA
United States
$460
- +
Product Description
Catalog Number:
AG003HJQ
Chemical Name:
2-Methoxybenzamide
CAS Number:
2439-77-2
Molecular Formula:
C8H9NO2
Molecular Weight:
151.1626
MDL Number:
MFCD00017120
IUPAC Name:
2-methoxybenzamide
InChI:
InChI=1S/C8H9NO2/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5H,1H3,(H2,9,10)
InChI Key:
MNWSGMTUGXNYHJ-UHFFFAOYSA-N
SMILES:
COc1ccccc1C(=O)N
EC Number:
219-465-8
UNII:
WRY8DDN8YC
NSC Number:
84232
Properties
Complexity:
147  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
151.063g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
151.165g/mol
Monoisotopic Mass:
151.063g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
52.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.8  
Literature
Title Journal
QSAR prediction of D2 receptor antagonistic activity of 6-methoxy benzamides. European journal of medicinal chemistry 20101101
Structure-activity relationships of anthraquinone derivatives derived from bromaminic acid as inhibitors of ectonucleoside triphosphate diphosphohydrolases (E-NTPDases). Purinergic signalling 20090301
Structural considerations for designing adenosine analogs as selective inhibitors of Trichomonas sp. glyceraldehyde-3- phosphate dehydrogenase. In silico biology 20070101
Thiourea-catalyzed asymmetric michael addition of activated methylene compounds to alpha,beta-unsaturated imides: dual activation of imide by intra- and intermolecular hydrogen bonding. Journal of the American Chemical Society 20060726
QSAR modeling on dopamine D2 receptor binding affinity of 6-methoxy benzamides. Farmaco (Societa chimica italiana : 1989) 20051001
Distamycin analogues with enhanced lipophilicity: synthesis and antimicrobial activity. Journal of medicinal chemistry 20040408
Properties