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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)-

ethyl 6-bromopyrazolo[1,5-a]pyrimidine-2-carboxylate

CCOC(=O)c1cc2n(n1)cc(cn2)Br Request for Quotation
Chemical Name: ethyl 6-bromopyrazolo[1,5-a]pyrimidine-2-carboxylate
CAS Number: 1005209-42-6
Product Number: AG00028S(AGN-PC-086G0K)
Synonyms:
MDL No:
Molecular Formula: C9H8BrN3O2
Molecular Weight: 270.0827

Identification/Properties

Computed Properties
Molecular Weight:
270.086g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
268.98g/mol
Monoisotopic Mass:
268.98g/mol
Topological Polar Surface Area:
56.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
252
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-2-carboxylate is a versatile compound used in chemical synthesis for its unique properties. With its bromine and carboxylate functional groups, this compound serves as a valuable building block in the creation of diverse organic molecules. In organic synthesis, it can be employed as a key intermediate for the development of pharmaceuticals, agrochemicals, and functional materials. Its structural features make it a valuable tool for creating complex molecular architectures through various synthetic pathways, enabling chemists to design and access novel compounds with potential applications across a range of industries. Additionally, the presence of the pyrazole and pyrimidine moieties confers specific reactivity and functionality to the molecule, allowing for selective transformations and efficient construction of target molecules with desired properties. By utilizing Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-2-carboxylate in chemical synthesis, researchers can unlock new avenues for the preparation of advanced materials and bioactive compounds, driving innovation in the field of organic chemistry.