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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, 7-(phenylmethoxy)-

c1ccc(cc1)COc1cccc2c1[nH]nc2 Request for Quotation
Chemical Name: 1H-Indazole, 7-(phenylmethoxy)-
CAS Number: 351210-09-8
Product Number: AG003NC5(AGN-PC-0747EI)
Synonyms:
MDL No: MFCD11110275
Molecular Formula: C14H12N2O
Molecular Weight: 224.2579

Identification/Properties

Properties
BP:
422.4±20.0°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid

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


7-(Benzyloxy)-1H-indazole is a versatile chemical compound that plays a crucial role in organic synthesis. With its unique structure and properties, this compound is widely utilized in the field of medicinal chemistry and pharmaceutical research. One of the key applications of 7-(Benzyloxy)-1H-indazole is as a building block in the synthesis of various biologically active compounds. Its benzyl group can serve as a protecting group, allowing for selective reactions to take place at specific positions within a molecule. This compound can be used as a precursor for the synthesis of indazole derivatives, which have shown promising pharmacological activities in drug discovery.Furthermore, 7-(Benzyloxy)-1H-indazole can undergo diverse chemical transformations, such as hydrogenation, functional group modifications, and cross-coupling reactions. These reactions enable the introduction of different substituents onto the indazole core, leading to the generation of novel compounds with tailored properties and enhanced biological activities.Overall, the application of 7-(Benzyloxy)-1H-indazole in chemical synthesis offers a valuable tool for organic chemists and researchers working towards the development of new drug candidates and bioactive molecules.