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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-Indazole, 1-acetyl-4-(phenylmethoxy)-

CC(=O)n1ncc2c1cccc2OCc1ccccc1 Request for Quotation
Chemical Name: 1H-Indazole, 1-acetyl-4-(phenylmethoxy)-
CAS Number: 65361-84-4
Product Number: AG00ELCK(AGN-PC-02SU8E)
Synonyms:
MDL No:
Molecular Formula: C16H14N2O2
Molecular Weight: 266.2946

Identification/Properties

Properties
BP:
453.3±37.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

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


1-(4-(Benzyloxy)-1H-indazol-1-yl)ethanone is a versatile compound widely used in chemical synthesis due to its unique reactivity and functional group compatibility. It serves as a valuable building block in the preparation of various organic molecules, especially in the field of medicinal chemistry and material science. In chemical synthesis, this compound can act as a key intermediate for the synthesis of complex heterocyclic compounds and pharmaceutical agents. Its indazole core provides structural diversity and potential for derivatization, making it suitable for the development of new drug candidates. Additionally, the benzyloxy group can be selectively modified or removed to access different derivatives with varying properties.Moreover, 1-(4-(Benzyloxy)-1H-indazol-1-yl)ethanone can participate in a range of reactions such as condensation, substitution, and reduction, allowing for efficient access to structurally diverse molecules. Its stability and compatibility with common reaction conditions make it a valuable tool for synthetic chemists seeking to design and optimize novel compounds for various applications.Overall, the application of 1-(4-(Benzyloxy)-1H-indazol-1-yl)ethanone in chemical synthesis offers tremendous potential for the creation of new materials, pharmaceuticals, and research compounds with tailored properties and functionalities.