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5441-02-1

5441-02-1 | N,N'-(2,6-Pyridinediyl)bis(acetamide)

CAS No: 5441-02-1 Catalog No: AG00DJ5P MDL No:MFCD00023425

Product Description

Catalog Number:
AG00DJ5P
Chemical Name:
N,N'-(2,6-Pyridinediyl)bis(acetamide)
CAS Number:
5441-02-1
Molecular Formula:
C9H11N3O2
Molecular Weight:
193.2025
MDL Number:
MFCD00023425
IUPAC Name:
N-(6-acetamidopyridin-2-yl)acetamide
InChI:
InChI=1S/C9H11N3O2/c1-6(13)10-8-4-3-5-9(12-8)11-7(2)14/h3-5H,1-2H3,(H2,10,11,12,13,14)
InChI Key:
DVKNWDFYHWHRML-UHFFFAOYSA-N
SMILES:
CC(=O)Nc1cccc(n1)NC(=O)C
NSC Number:
20559

Properties

Complexity:
208  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
193.085g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
193.206g/mol
Monoisotopic Mass:
193.085g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
71.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.1  

Literature

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Barbituric acid as a substituent at aryl methylium ions. The Journal of organic chemistry 20060929
Microsphere-based protease assays and screening application for lethal factor and factor Xa. Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501
The electrochemically-tuneable interactions between flavin-functionalised C60 derivatives and 2,6-diethylamidopyridine. Chemical communications (Cambridge, England) 20050814
The electrochemically tuneable recognition properties of an electropolymerised flavin derivative. Chemical communications (Cambridge, England) 20041207
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Model systems for flavoenzyme activity: flavin-functionalised SAMs as models for probing redox modulation through hydrogen bonding. Chemical communications (Cambridge, England) 20031007

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