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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

5-amino-1-(oxan-4-yl)pyrazole-4-carboxamide

NC(=O)c1cnn(c1N)C1CCOCC1 Request for Quotation
Chemical Name: 5-amino-1-(oxan-4-yl)pyrazole-4-carboxamide
CAS Number: 1082745-50-3
Product Number: AG0083V9(AGN-PC-0687IP)
Synonyms:
MDL No:
Molecular Formula: C9H14N4O2
Molecular Weight: 210.2331

Identification/Properties

Computed Properties
Molecular Weight:
210.237g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
210.112g/mol
Monoisotopic Mass:
210.112g/mol
Topological Polar Surface Area:
96.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
242
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Amino-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazole-4-carboxamide is a versatile compound utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its structural characteristics and functional groups. In chemical synthesis, this compound can undergo a range of reactions such as acylation, alkylation, and condensation to introduce different moieties and form complex structures. Its presence in the synthesis process can lead to the creation of novel compounds with diverse biological activities or material properties, making it a valuable tool for organic chemists and researchers in drug discovery and material science.