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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-Indole-2-methanol, 6-chloro-

OCc1cc2c([nH]1)cc(cc2)Cl Request for Quotation
Chemical Name: 1H-Indole-2-methanol, 6-chloro-
CAS Number: 53590-58-2
Product Number: AG00DC5T(AGN-PC-00TXOA)
Synonyms:
MDL No:
Molecular Formula: C9H8ClNO
Molecular Weight: 181.61892

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (6-Chloro-1H-indol-2-yl)methanol is a versatile building block in chemical synthesis due to its unique structure and reactivity. Thanks to the presence of both an indole ring and a hydroxyl functional group, this compound is commonly used in the production of various pharmaceuticals, agrochemicals, and organic materials.In organic synthesis, (6-Chloro-1H-indol-2-yl)methanol can serve as a key intermediate for the preparation of complex molecules with indole moieties. Its chloro substituent provides opportunities for further derivatization, allowing chemists to introduce additional functionality into the molecule. The hydroxyl group can participate in a range of chemical reactions, such as oxidation, reduction, and esterification, expanding the compound's synthetic utility.One notable application of (6-Chloro-1H-indol-2-yl)methanol is in the synthesis of indole-based pharmaceutical compounds. Indole derivatives are known for their diverse biological activities, including anticancer, antibacterial, and antiviral properties. By incorporating (6-Chloro-1H-indol-2-yl)methanol into the chemical synthesis of these molecules, researchers can access novel drug candidates with tailored properties and improved pharmacokinetics.Furthermore, the incorporation of (6-Chloro-1H-indol-2-yl)methanol into the design of bioactive agrochemicals can lead to the development of environmentally friendly pesticides or growth regulators. The indole scaffold has been shown to exhibit plant growth-promoting effects and can enhance the defense mechanisms of crops against pathogens. By leveraging the reactivity of (6-Chloro-1H-indol-2-yl)methanol, chemists can create innovative solutions for sustainable agriculture practices.Overall, the versatility and reactivity of (6-Chloro-1H-indol-2-yl)methanol make it a valuable tool in chemical synthesis, enabling the construction of complex molecules with indole functionalities for applications in pharmaceuticals, agrochemicals, and materials science.