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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)-

3-Chloro-5-hydroxy-1H-indazole

Oc1ccc2c(c1)c(Cl)n[nH]2 Request for Quotation
Chemical Name: 3-Chloro-5-hydroxy-1H-indazole
CAS Number: 885519-34-6
Product Number: AG003J9G(AGN-PC-0WAFSA)
Synonyms:
MDL No:
Molecular Formula: C7H5ClN2O
Molecular Weight: 168.5804

Identification/Properties

Properties
Storage:
2-8℃;Keep in dry area;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Chloro-1H-indazol-5-ol, also known as $name$, is a versatile chemical compound widely used in chemical synthesis. One prominent application of this compound is in the field of pharmaceutical research and development. Due to its unique structure and reactivity, $name$ serves as a valuable building block for the synthesis of various bioactive molecules and pharmaceutical intermediates. Its incorporation in drug design projects has shown promising results in the development of novel therapies for a range of diseases. In addition, $name$ is also utilized in the synthesis of advanced materials such as polymers and functionalized nanoparticles, where its specific chemical properties play a crucial role in determining the final characteristics of the materials produced. Furthermore, in the field of organic chemistry, the reactivity of 3-Chloro-1H-indazol-5-ol has been exploited for the construction of complex molecular structures through diverse synthetic pathways, making it a key reagent in modern chemical synthesis.