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Pyridazin-3-amine

CAS No.:
5469-70-5
Catalog Number:
AG0033LI
Molecular Formula:
C4H5N3
Molecular Weight:
95.1026
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$32
- +
10g
95%
In Stock USA
United States
$50
- +
25g
98%
In Stock USA
United States
$112
- +
100g
98%
In Stock USA
United States
$313
- +
500g
98%
In Stock USA
United States
$1225
- +
Product Description
Catalog Number:
AG0033LI
Chemical Name:
Pyridazin-3-amine
CAS Number:
5469-70-5
Molecular Formula:
C4H5N3
Molecular Weight:
95.1026
MDL Number:
MFCD01529869
IUPAC Name:
pyridazin-3-amine
InChI:
InChI=1S/C4H5N3/c5-4-2-1-3-6-7-4/h1-3H,(H2,5,7)
InChI Key:
LETVJWLLIMJADE-UHFFFAOYSA-N
SMILES:
Nc1cccnn1
NSC Number:
25228
Properties
Complexity:
54.9  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
95.048g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
95.105g/mol
Monoisotopic Mass:
95.048g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
51.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.2  
Literature
Title Journal
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Polyfunctional nitriles in organic syntheses: a novel route to aminopyrroles, pyridazines and pyrazolo[3,4-c]pyridazines. Molecules (Basel, Switzerland) 20090216
A novel and convenient protocol for synthesis of pyridazines. Organic letters 20090115
R75761, a lead compound for the development of antiviral drugs in late stage poliomyelitis eradication strategies and beyond. Antiviral research 20080601
Privileged structures: a useful concept for the rational design of new lead drug candidates. Mini reviews in medicinal chemistry 20071101
Use of 4-bromo pyridazine 3,6-dione for building 3-amino pyridazine libraries. Molecular diversity 20060801
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Aminopyridazines attenuate hippocampus-dependent behavioral deficits induced by human beta-amyloid in a murine model of neuroinflammation. Journal of molecular neuroscience : MN 20040101
Aminopyridazines inhibit beta-amyloid-induced glial activation and neuronal damage in vivo. Neurobiology of aging 20040101
An aminopyridazine-based inhibitor of a pro-apoptotic protein kinase attenuates hypoxia-ischemia induced acute brain injury. Bioorganic & medicinal chemistry letters 20031020
Discovery of new chemical classes of synthetic ligands that suppress neuroinflammatory responses. Journal of molecular neuroscience : MN 20020101
Serotonin receptor and transporter ligands - current status. Current medicinal chemistry 20010701
Structure-based 3D QSAR and design of novel acetylcholinesterase inhibitors. Journal of computer-aided molecular design 20010501
Properties