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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)-

Pyrazolo[1,5-a]pyrimidine-6-carbonitrile, 7-amino-

N#Cc1cnc2n(c1N)ncc2 Request for Quotation
Chemical Name: Pyrazolo[1,5-a]pyrimidine-6-carbonitrile, 7-amino-
CAS Number: 89975-57-5
Product Number: AG003ND0(AGN-PC-0KLFQX)
Synonyms:
MDL No: MFCD00104599
Molecular Formula: C7H5N5
Molecular Weight: 159.1481

Identification/Properties

Properties
MP:
306-308℃(Solv: ethanol (64-17-5))
Storage:
Light sensitive;Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
159.152g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
159.054g/mol
Monoisotopic Mass:
159.054g/mol
Topological Polar Surface Area:
80A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
219
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:
Danger
UN#:
2811
Hazard Statements:
H301-H315-H319-H335
Precautionary Statements:
P261-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Aminopyrazolo[1,5-a]pyrimidine-6-carbonitrile is a versatile compound commonly used in chemical synthesis as a key intermediate in the production of pharmaceuticals, agrochemicals, and various functional materials. With its unique structure and reactivity, this molecule serves as a valuable building block in the synthesis of various heterocyclic compounds and complex organic molecules.In chemical synthesis, 7-Aminopyrazolo[1,5-a]pyrimidine-6-carbonitrile can undergo diverse transformations, including substitution reactions, condensation reactions, and cyclization reactions, leading to the formation of structurally diverse compounds with potential biological activities. Its presence in the molecular structure imparts valuable properties and functionalities to the final products, making it a sought-after compound in the pharmaceutical and agrochemical industries.Moreover, 7-Aminopyrazolo[1,5-a]pyrimidine-6-carbonitrile can be modified through derivatization processes to introduce specific functional groups or enhance its solubility, stability, and bioavailability. This versatility allows for the tailored design and synthesis of compounds with optimized characteristics for targeted applications.Overall, the application of 7-Aminopyrazolo[1,5-a]pyrimidine-6-carbonitrile in chemical synthesis plays a crucial role in the development of novel compounds with potential therapeutic, agricultural, and material science applications.