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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)-

1H-Pyrazolo[4,3-b]pyridine, 7-chloro-5-methyl-

Cc1cc(Cl)c2c(n1)cn[nH]2 Request for Quotation
Chemical Name: 1H-Pyrazolo[4,3-b]pyridine, 7-chloro-5-methyl-
CAS Number: 94220-38-9
Product Number: AG0065WA(AGN-PC-00DZUB)
Synonyms:
MDL No:
Molecular Formula: C7H6ClN3
Molecular Weight: 167.5956

Identification/Properties

Properties
BP:
307.317 °C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
167.596g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
167.025g/mol
Monoisotopic Mass:
167.025g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
153
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1H-Pyrazolo[4,3-b]pyridine, 7-chloro-5-methyl- is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the creation of various complex organic molecules due to its structural features and functional groups. Its presence in a synthesis pathway can introduce specific regioselectivity and functionalization to the desired end product. The 7-chloro and 5-methyl substituents on the pyrazolo[4,3-b]pyridine ring impart specific characteristics that enable precise control over the reaction outcomes. Researchers and chemists utilize this compound strategically to access diverse chemical space and achieve tailored molecular structures for pharmaceuticals, agrochemicals, and materials science applications.