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Home Aldehydes 2-Amino-pyridine-3-carbaldehyde oxime, HCl

2-Amino-pyridine-3-carbaldehyde oxime, HCl

CAS No.:
653584-65-7
Catalog Number:
AG003GJY
Molecular Formula:
C6H8ClN3O
Molecular Weight:
173.6002
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
25mg
95%(HPLC)
In Stock USA
United States
$61
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100mg
95%(HPLC)
In Stock USA
United States
$119
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250mg
95%(HPLC)
In Stock USA
United States
$221
- +
1g
95%(HPLC)
In Stock USA
United States
$436
- +
5g
95%(HPLC)
In Stock USA
United States
$1269
- +
Product Description
Catalog Number:
AG003GJY
Chemical Name:
2-Amino-pyridine-3-carbaldehyde oxime, HCl
CAS Number:
653584-65-7
Molecular Formula:
C6H8ClN3O
Molecular Weight:
173.6002
MDL Number:
MFCD06659001
IUPAC Name:
(NE)-N-[(2-aminopyridin-3-yl)methylidene]hydroxylamine;hydrochloride
InChI:
InChI=1S/C6H7N3O.ClH/c7-6-5(4-9-10)2-1-3-8-6;/h1-4,10H,(H2,7,8);1H/b9-4+;
InChI Key:
DGNBEVBYMQDDDO-JOKMOOFLSA-N
SMILES:
Nc1ncccc1/C=N/O.Cl
Properties
Complexity:
126  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1  
Exact Mass:
173.036g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
173.6g/mol
Monoisotopic Mass:
173.036g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
71.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Literature
Title Journal
Detection of enzymatically generated hydrogen peroxide by metal-based fluorescent probe. Analytical chemistry 20111215
Laser-induced mixing in microfluidic channels. Analytical chemistry 20070615
Measurement of enzyme kinetics using a continuous-flow microfluidic system. Analytical chemistry 20030701
A fluorometric assay for detection of lysyl oxidase enzyme activity in biological samples. Analytical biochemistry 20020115
In vitro quantitation of biological superoxide and hydrogen peroxide generation. Methods in enzymology 20020101
Hydrogen peroxide formation during iron deposition in horse spleen ferritin using O2 as an oxidant. Biochemistry 20010320
Properties