1. Home
  2. 2-(6-bromo-1H-indol-3-yl)ethanol

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

2-(6-bromo-1H-indol-3-yl)ethanol

OCCc1c[nH]c2c1ccc(c2)Br Request for Quotation
Chemical Name: 2-(6-bromo-1H-indol-3-yl)ethanol
CAS Number: 214915-72-7
Product Number: AG00BTDK(AGN-PC-022XGF)
Synonyms:
MDL No:
Molecular Formula: C10H10BrNO
Molecular Weight: 240.0965

Identification/Properties

Computed Properties
Molecular Weight:
240.1g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
238.995g/mol
Monoisotopic Mass:
238.995g/mol
Topological Polar Surface Area:
36A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
176
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

Request for Quotation

Customer Feedback

Chemical Structure


2-(6-Bromo-1H-indol-3-yl)ethanol is a versatile compound widely used in chemical synthesis for its unique properties. It serves as a valuable building block in the production of pharmaceuticals, agrochemicals, and materials science. Due to its functional groups, this compound can undergo various chemical reactions, such as acylation, alkylation, and oxidation, leading to the synthesis of complex organic molecules. Its indole moiety imparts aromaticity and electron-rich properties, making it an important intermediate in the synthesis of bioactive compounds. Additionally, the presence of the hydroxyl group enhances its reactivity and diversifies its applications in organic transformations.