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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, 3-bromo-5,7-dichloro-

Clc1cc(Cl)n2c(n1)c(Br)cn2 Request for Quotation
Chemical Name: Pyrazolo[1,5-a]pyrimidine, 3-bromo-5,7-dichloro-
CAS Number: 114040-06-1
Product Number: AG000ADN(AGN-PC-002F9B)
Synonyms:
MDL No:
Molecular Formula: C6H2BrCl2N3
Molecular Weight: 266.9102

Identification/Properties

Computed Properties
Molecular Weight:
266.907g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
264.881g/mol
Monoisotopic Mass:
264.881g/mol
Topological Polar Surface Area:
30.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
182
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-Bromo-5,7-dichloropyrazolo[1,5-a]pyrimidine is a versatile compound widely used in chemical synthesis as a key building block. It serves as a valuable intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. This compound enables the efficient incorporation of specific functional groups and structural motifs into target molecules, allowing for the synthesis of complex and biologically active compounds. Its unique reactivity and structural features make it a valuable tool in the hands of synthetic chemists for the creation of novel compounds with diverse applications.