5-Methyl-1H-pyrazol-3-amine
Suppliers
Names
[ CAS No. ]:
31230-17-8
[ Name ]:
5-Methyl-1H-pyrazol-3-amine
[Synonym ]:
3,5-AMP
3-methyl-5-amino-1H-pyrazole
5-METHYL-3-PYRAZOLAMINE
3-Methyl-1H-pyrazol-5-amine
MFCD00051640
1H-Pyrazol-3-amine, 5-methyl-
5-Methyl-1H-pyrazol-3-amine
5(3)-amino-3(5)-methylpyrazole
3-(methyl)-1H-pyrazol-5-amine
3-Amino-5-Methyl-1H-Pyrazole
5-amino-3-methylpyrazole
3(5)-amino-5(3)-methylpyrazole
3,1-AMP
5-Methylpyrazol-3-amine
(3-methyl-1H-pyrazol-5-yl)amine
3(5)-amino-5(3)-methyl-NH-pyrazole
5-Metyl-3-aminopyrazole
Chemical & Physical Properties
[ Density]:
1.2±0.1 g/cm3
[ Boiling Point ]:
357.0±0.0 °C at 760 mmHg
[ Melting Point ]:
45-47 °C(lit.)
[ Molecular Formula ]:
C4H7N3
[ Molecular Weight ]:
97.12
[ Flash Point ]:
169.5±9.5 °C
[ Exact Mass ]:
97.063995
[ PSA ]:
54.70000
[ LogP ]:
0.17
[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C
[ Index of Refraction ]:
1.617
[ Storage condition ]:
-20?C Freezer
[ Stability ]:
Light Sensitive
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi:Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36-S37/39
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Articles
Inorg. Chem. 40(17) , 4409-19, (2001)
The use of 3-aminopyrazole derivatives as beta-sheet templates is investigated using a series of ferrocenoyl (Fc)-dipeptides (Fc-Gly(2)-OEt, Fc-Ala(2)-OBzl, Fc-Leu-Phe-OMe, Fc-Val-Phe-OMe, Fc-Phe(2)-O...
Chemistry 13(3) , 854-61, (2007)
Complexation of the amino- and carboxyl-protected tripeptide Piv-L-Val-L-Val-L-Val-tBu with 3-methylpyrazole and 3-amino-5-methylpyrazole was studied by low-temperature NMR experiments in a freonic so...
Synthesis of partially hydrogenated pyrazolo [3, 4-b] quinolinones by condensation of 3-amino-5-methylpyrazole with aromatic aldehydes and dimedone. Lipson VV, et al.Russ. J. Org. Chem. 42(7) , 1015-21, (2006)