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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)-

3-(Boc-aminomethyl)pyrazole

O=C(OC(C)(C)C)NCc1cc[nH]n1 Request for Quotation
Chemical Name: 3-(Boc-aminomethyl)pyrazole
CAS Number: 1251033-82-5
Product Number: AG000N6X(AGN-PC-0WAGRI)
Synonyms:
MDL No:
Molecular Formula: C9H15N3O2
Molecular Weight: 197.2343

Identification/Properties

Computed Properties
Molecular Weight:
197.238g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
197.116g/mol
Monoisotopic Mass:
197.116g/mol
Topological Polar Surface Area:
67A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
201
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


3-(Boc-aminomethyl)pyrazole is a versatile compound commonly employed in chemical synthesis as a key building block. Its unique structure and reactivity make it an essential component in the creation of various complex molecules. One of its primary applications is in the production of pharmaceutical intermediates, where it serves as a crucial starting material for the synthesis of bioactive compounds and drug candidates. Additionally, 3-(Boc-aminomethyl)pyrazole is utilized in the development of agrochemicals, materials science, and other research areas that require the precise manipulation of molecular structures. Its compatibility with a wide range of reactions and functional group transformations makes it a valuable tool for synthetic chemists seeking to access diverse chemical space and explore novel molecular architectures.