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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)-

1-benzyl-4-(chloromethyl)pyrazole;hydrochloride

ClCc1cnn(c1)Cc1ccccc1.Cl Request for Quotation
Chemical Name: 1-benzyl-4-(chloromethyl)pyrazole;hydrochloride
CAS Number: 861135-54-8
Product Number: AG003DZP(AGN-PC-09S1SY)
Synonyms:
MDL No: MFCD08234806
Molecular Formula: C11H12Cl2N2
Molecular Weight: 243.1324

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
243.131g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
242.038g/mol
Monoisotopic Mass:
242.038g/mol
Topological Polar Surface Area:
17.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
169
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Benzyl-4-(chloromethyl)-1H-pyrazole hydrochloride is a highly versatile compound widely utilized in chemical synthesis. Its unique structure and reactivity make it a valuable building block for the creation of various organic compounds, particularly in the pharmaceutical and agrochemical industries.In chemical synthesis, 1-Benzyl-4-(chloromethyl)-1H-pyrazole hydrochloride is commonly employed as a key intermediate for the production of heterocyclic compounds. Its chloromethyl group allows for selective functionalization, enabling the introduction of diverse chemical moieties to tailor the compound for specific applications.Furthermore, the benzyl group in 1-Benzyl-4-(chloromethyl)-1H-pyrazole hydrochloride provides stability and enhances the compound's compatibility with a wide range of reaction conditions. This versatility makes it an essential component in the synthesis of complex molecules with defined structural features.Overall, 1-Benzyl-4-(chloromethyl)-1H-pyrazole hydrochloride plays a crucial role in chemical synthesis by serving as a strategic building block for the construction of diverse organic compounds with potential applications in pharmaceuticals, agrochemicals, and other industries.