2107-69-9 | 5,6-Dimethoxy-1-indanone

Packsize	Purity	Availability	Price	Discounted Price
5g	96%	in stock	$13.00	$9.00
25g	96%	in stock	$33.00	$23.00
100g	96%	in stock	$88.00	$62.00
500g	96%	in stock	$249.00	$175.00

Description

• Catalog Number: AB20245
• Chemical Name: 5,6-Dimethoxy-1-indanone
• CAS Number: 2107-69-9
• Molecular Formula: C11H12O3
• Molecular Weight: 192.2112
• MDL Number: MFCD00003790
• SMILES: COc1cc2C(=O)CCc2cc1OC
• NSC Number: 401450

Computed Properties

• Complexity: 227
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• XLogP3: 1.6

Literature

• Antiviral activity against the hepatitis C virus (HCV) of 1-indanone thiosemicarbazones and their inclusion complexes with hydroxypropyl-β-cyclodextrin.

  European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences 20121009

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101

• (2E)-2-Benzyl-idene-5,6-dimethoxy-indan-1-one.

  Acta crystallographica. Section E, Structure reports online 20101001

• Thienylhalomethylketones: Irreversible glycogen synthase kinase 3 inhibitors as useful pharmacological tools.

  Bioorganic & medicinal chemistry 20091001

• Methyl 5,6-dimeth-oxy-1H-indole-2-carboxyl-ate.

  Acta crystallographica. Section E, Structure reports online 20091001

• Photochemical synthesis of substituted indan-1-ones related to donepezil.

  Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20080501

• Simple and regioselective bromination of 5,6-disubstituted-indan-1-ones with Br2 under acidic and basic conditions.

  Molecules (Basel, Switzerland) 20070129

• Dopamine D(3) receptor antagonists. 1. Synthesis and structure-activity relationships of 5,6-dimethoxy-N-alkyl- and N-alkylaryl-substituted 2-aminoindans.

  Journal of medicinal chemistry 20011220