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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)-

1H-Pyrazol-3-amine, 5-(1,1-dimethylethyl)-

CC(c1[nH]nc(c1)N)(C)C Request for Quotation
Chemical Name: 1H-Pyrazol-3-amine, 5-(1,1-dimethylethyl)-
CAS Number: 82560-12-1
Product Number: AG0033L8(AGN-PC-0JSASZ)
Synonyms:
MDL No: MFCD00082631
Molecular Formula: C7H13N3
Molecular Weight: 139.1982

Identification/Properties

Properties
MP:
60 °C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
139.202g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
139.111g/mol
Monoisotopic Mass:
139.111g/mol
Topological Polar Surface Area:
54.7A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
117
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Amino-5-tert-butylpyrazole is a versatile chemical compound that finds a wide range of applications in chemical synthesis. One of its key uses is as a building block in the preparation of various pharmaceuticals and agrochemicals. Its unique structure and properties make it a valuable intermediate in the synthesis of complex organic molecules.In chemical synthesis, 3-Amino-5-tert-butylpyrazole can serve as a nucleophilic reagent in organic reactions, particularly in the formation of C-N bonds. Its amino group can undergo a variety of transformations, such as acylation, alkylation, and condensation reactions, allowing for the introduction of various functional groups into target molecules.Furthermore, 3-Amino-5-tert-butylpyrazole can act as a chelating ligand in coordination chemistry, forming stable metal complexes that have potential applications in catalysis and material science.Overall, the versatility of 3-Amino-5-tert-butylpyrazole makes it a valuable tool in the toolbox of synthetic chemists for the efficient construction of diverse organic compounds with tailored properties and functionalities.