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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)-

5-(chloromethyl)-2-pyrazol-1-ylpyridine

ClCc1ccc(nc1)n1cccn1 Request for Quotation
Chemical Name: 5-(chloromethyl)-2-pyrazol-1-ylpyridine
CAS Number: 748796-39-6
Product Number: AG005GMG(AGN-PC-0140PS)
Synonyms:
MDL No:
Molecular Formula: C9H8ClN3
Molecular Weight: 193.6329

Identification/Properties

Properties
BP:
336.074°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Stability:
Light Sensitive
Computed Properties
Molecular Weight:
193.634g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
193.041g/mol
Monoisotopic Mass:
193.041g/mol
Topological Polar Surface Area:
30.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
165
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:
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


5-(Chloromethyl)-2-(1H-pyrazol-1-yl)pyridine is a versatile compound commonly used in chemical synthesis for its unique properties. This molecule acts as a valuable building block in the synthesis of various organic compounds due to its functional groups and reactivity. 
One of the significant applications of 5-(Chloromethyl)-2-(1H-pyrazol-1-yl)pyridine is in the preparation of pyrazole-containing pharmaceuticals and agrochemicals. The presence of the pyrazole ring in the molecule makes it an essential intermediate for the synthesis of bioactive compounds with diverse pharmacological activities. Additionally, the chloromethyl group provides a site for further functionalization, enabling the introduction of various substituents to modulate the properties of the final product. 
Moreover, this compound can also participate in cross-coupling reactions and serve as a precursor for the introduction of other functional groups, making it a valuable tool in organic synthesis. Its versatility and reactivity make 5-(Chloromethyl)-2-(1H-pyrazol-1-yl)pyridine a crucial component in the development of new molecules with potential applications in the fields of medicine, agriculture, and materials science.