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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)-

4-(chloromethyl)-1H-indazole

ClCc1cccc2c1cn[nH]2 Request for Quotation
Chemical Name: 4-(chloromethyl)-1H-indazole
CAS Number: 944898-78-6
Product Number: AG00H6D2(AGN-PC-0ALPV8)
Synonyms:
MDL No:
Molecular Formula: C8H7ClN2
Molecular Weight: 166.6076

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
166.608g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
166.03g/mol
Monoisotopic Mass:
166.03g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
140
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:
Danger
UN#:
3261
Hazard Statements:
H302-H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Chloromethyl)-1H-indazole is a versatile compound widely used in chemical synthesis due to its unique reactivity and structural properties. One of the key applications of this compound is in the synthesis of pharmaceutical intermediates, where it serves as a valuable building block for the creation of complex organic molecules. In organic chemistry, 4-(Chloromethyl)-1H-indazole can be utilized in various reactions such as nucleophilic substitution, Suzuki coupling, and Grignard reactions. By incorporating this compound into different synthetic pathways, chemists can access a wide range of structurally diverse compounds with potential biological activities. Additionally, the chloromethyl group in 4-(Chloromethyl)-1H-indazole offers a reactive site for further functionalization, allowing for the introduction of different substituents to tailor the properties of the final products. This flexibility makes it a valuable tool in the design and synthesis of novel compounds for drug discovery and materials science research. Overall, the application of 4-(Chloromethyl)-1H-indazole in chemical synthesis enables chemists to access new molecules and explore the boundaries of organic chemistry, opening up avenues for innovation and discovery in various fields.