1. Home
  2. Acetamide, N-(6-bromo-2,3-dihydro-1H-inden-5-yl)-

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)-

Acetamide, N-(6-bromo-2,3-dihydro-1H-inden-5-yl)-

CC(=O)Nc1cc2CCCc2cc1Br Request for Quotation
Chemical Name: Acetamide, N-(6-bromo-2,3-dihydro-1H-inden-5-yl)-
CAS Number: 157701-33-2
Product Number: AG001PMX(AGN-PC-0N3TQ4)
Synonyms:
MDL No:
Molecular Formula: C11H12BrNO
Molecular Weight: 254.1231

Identification/Properties

Computed Properties
Molecular Weight:
254.127g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
253.01g/mol
Monoisotopic Mass:
253.01g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
231
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


The compound N-(6-Bromo-2,3-dihydro-1H-inden-5-yl)acetamide is a versatile building block in chemical synthesis due to its unique structural features. It serves as a key intermediate in the preparation of various biologically active molecules, pharmaceuticals, and agrochemicals. Its reactivity allows for selective functionalization at different positions, enabling the creation of diverse chemical libraries for drug discovery and development. Additionally, the presence of the bromo substituent offers a convenient handle for further derivatization through various cross-coupling reactions, facilitating the synthesis of complex molecular structures with high efficiency and precision.