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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-3-(chloromethyl)indazole

ClCc1nn(c2c1cccc2)Cc1ccccc1 Request for Quotation
Chemical Name: 1-benzyl-3-(chloromethyl)indazole
CAS Number: 131427-22-0
Product Number: AG000W5R(AGN-PC-09OWR0)
Synonyms:
MDL No: MFCD20134218
Molecular Formula: C15H13ClN2
Molecular Weight: 256.7301

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
256.733g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
256.077g/mol
Monoisotopic Mass:
256.077g/mol
Topological Polar Surface Area:
17.8A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
265
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


1-Benzyl-3-(chloromethyl)-1H-indazole, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the creation of various organic molecules with pharmaceutical, agricultural, and material science applications.In chemical synthesis, $name$ plays a crucial role as a versatile intermediate that can undergo diverse reactions to yield a wide range of functionalized products. Its chloromethyl group enables selective transformations through nucleophilic substitution, making it valuable for introducing different functional groups into the molecular structure.One common application of 1-Benzyl-3-(chloromethyl)-1H-indazole is in the synthesis of biologically active compounds, such as pharmaceutical agents, agrochemicals, and specialized materials. By strategically incorporating this compound into chemical reactions, chemists can access new molecules with tailored properties and activities.Furthermore, the unique structural features of $name$ make it a valuable tool for the development of novel chemical entities and the exploration of structure-activity relationships. Its presence in the molecular scaffold can impart specific physicochemical characteristics that are vital for the desired functionality of the final product.Overall, 1-Benzyl-3-(chloromethyl)-1H-indazole is a versatile and essential component in modern chemical synthesis, enabling the efficient construction of complex molecules with diverse applications across various industries.