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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)-

7-bromo-1H-pyrazolo[3,4-c]pyridine

Brc1nccc2c1n[nH]c2 Request for Quotation
Chemical Name: 7-bromo-1H-pyrazolo[3,4-c]pyridine
CAS Number: 957760-11-1
Product Number: AG00IJG1(AGN-PC-0J0Y6B)
Synonyms:
MDL No:
Molecular Formula: C6H4BrN3
Molecular Weight: 198.0201

Identification/Properties

Computed Properties
Molecular Weight:
198.023g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
196.959g/mol
Monoisotopic Mass:
196.959g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
130
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:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Bromo-1H-pyrazolo[3,4-c]pyridine is a versatile building block in chemical synthesis due to its unique structure and reactivity. This compound serves as an important intermediate in the preparation of various organic molecules with valuable properties. In organic synthesis, 7-Bromo-1H-pyrazolo[3,4-c]pyridine can be utilized as a key starting material for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its bromine substitution provides an opportunity for further functionalization through cross-coupling reactions, allowing for the introduction of different substituents at specific positions on the pyrazolo[3,4-c]pyridine scaffold. This enables the synthesis of diverse chemical compounds with tailored functionalities and potential biological activities. Additionally, the presence of the pyridine ring in 7-Bromo-1H-pyrazolo[3,4-c]pyridine imparts aromatic properties, making it a valuable component in the design and construction of complex organic molecules.