3-Aminopyrazole-4-carboxylic acid
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3-Aminopyrazole-4-carboxylic acid
structure -
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CAS No:
41680-34-6
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Formula:
C4H5N3O2
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Chemical Name:
3-Aminopyrazole-4-carboxylic acid
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Synonyms:
RARECHEM AL BO 0208;3-amino-1h-pyrazole-4-carboxylicaci;3-amino-4-carboxypyrazole;3-amino-4-pyrazolecarboxylicaci;3-AMINO-4-PYRAZOLECARBOXYLIC ACID;3-AMINOPYRAZOLE-4-CARBOXYLIC ACID;5-AMINO-4-PYRAZOLECARBOXYLIC ACID;3-Amino-1H-pyrazol-4-carboxylic acid
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CAS No:
3-Aminopyrazole-4-carboxylic acid Basic Attributes
127.1
127.10
255-493-7
0XI8D7H29Z
89246
DTXSID60194494
White
29339900
Characteristics
92
-0.1
1.4748 (rough estimate)
135 °C (dec.) (lit.)
235.85°C (rough estimate)
257.8±25.9 °C
1.5000 (estimate)
Refrigerator (+4°C)
15.28±0.50(Predicted)
2-8°C
Safety Information
NONH for all modes of transport
3
Xi
26-37/39
UQ6390000
Xi
P261-P305 + P351 + P338
36/37/38
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 44 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
3-Aminopyrazole-4-carboxylic acid Use and Manufacturing
3-Amino-1H-pyrazole-4-carboxylic Acid, is a heterocyclic building block used for the synthesis of more complex pharmaceutical and biologically active compounds, including inhibitors. It can be used for the preparation of some impurities and/or degradation products of Zaleplon (Z145000), and also for Arylsulfonamidopiperidone derivatives as a novel class of factor Xa inhibitors.
Computed Properties
Molecular Weight:127.10
XLogP3:-0.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:127.038176411
Monoisotopic Mass:127.038176411
Topological Polar Surface Area:92
Heavy Atom Count:9
Complexity:127
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Recommended Suppliers of 3-Aminopyrazole-4-carboxylic acid
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3-Aminopyrazole-4-carboxylic acid
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