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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)-

(6-bromo-1H-indol-2-yl)methanol

OCc1cc2c([nH]1)cc(cc2)Br Request for Quotation
Chemical Name: (6-bromo-1H-indol-2-yl)methanol
CAS Number: 923197-75-5
Product Number: AG00GUT5(AGN-PC-00N3TV)
Synonyms:
MDL No:
Molecular Formula: C9H8BrNO
Molecular Weight: 226.0699

Identification/Properties

Computed Properties
Molecular Weight:
226.073g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
224.979g/mol
Monoisotopic Mass:
224.979g/mol
Topological Polar Surface Area:
36A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
165
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Bromo-1H-indol-2-yl)methanol, a versatile compound commonly used in chemical synthesis, serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and chemical intermediates. Known for its ability to participate in a wide range of reactions, this compound plays a crucial role in the development of new drug candidates and other valuable compounds. In organic synthesis, it is frequently employed as a nucleophilic reagent for the formation of carbon-carbon and carbon-heteroatom bonds. Additionally, its unique structural features make it a valuable starting material for the preparation of diverse heterocyclic compounds through various synthetic pathways. This compound's reactivity and compatibility with a variety of functional groups make it an indispensable tool for chemists working in the field of medicinal and organic chemistry.