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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)-

1-tert-butyl-3-[(3-methylphenyl)methyl]pyrazolo[3,4-d]pyrimidin-4-amine

Cc1cccc(c1)Cc1nn(c2c1c(N)ncn2)C(C)(C)C Request for Quotation
Chemical Name: 1-tert-butyl-3-[(3-methylphenyl)methyl]pyrazolo[3,4-d]pyrimidin-4-amine
CAS Number: 956025-83-5
Product Number: AG005ZPC(AGN-PC-04SVX7)
Synonyms:
MDL No: MFCD11655904
Molecular Formula: C17H21N5
Molecular Weight: 295.3821

Identification/Properties

Properties
MP:
130-132°C
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
295.39g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
295.18g/mol
Monoisotopic Mass:
295.18g/mol
Topological Polar Surface Area:
69.6A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
380
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


4-AMINO-1-TERT-BUTYL-3-(3-METHYLBENZYL)PYRAZOLO[3,4-D]PYRIMIDINE is a versatile compound widely utilized in chemical synthesis due to its unique structural properties. In the field of organic chemistry, this compound serves as a key building block for the synthesis of various heterocyclic compounds and pharmaceutical intermediates. Its substitution pattern and functional groups make it a valuable reagent for the creation of novel molecules with potential biological activities.One of the prominent applications of 4-AMINO-1-TERT-BUTYL-3-(3-METHYLBENZYL)PYRAZOLO[3,4-D]PYRIMIDINE is in the development of new drug candidates through medicinal chemistry. By incorporating this compound into molecular structures, researchers can explore its interactions with biological targets and evaluate its pharmacological properties. Additionally, its presence in molecular frameworks can enhance the stability and selectivity of drug molecules, making them more effective in therapeutic applications.Furthermore, in the field of materials science, 4-AMINO-1-TERT-BUTYL-3-(3-METHYLBENZYL)PYRAZOLO[3,4-D]PYRIMIDINE is utilized for the construction of functional polymers and advanced materials. Its reactivity and stability make it a suitable building block for designing polymers with specific properties, such as conductivity, optical activity, or mechanical strength. By incorporating this compound into polymer chains, researchers can tailor the material characteristics to meet various industrial or technological needs.Overall, the versatility and utility of 4-AMINO-1-TERT-BUTYL-3-(3-METHYLBENZYL)PYRAZOLO[3,4-D]PYRIMIDINE make it a valuable tool in the realm of chemical synthesis, enabling the development of diverse molecules with potential applications in drug discovery, materials science, and other scientific fields.