2235-15-6 | 1-Acenaphthenone

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$25.00	$17.00
1g	97%	in stock	$32.00	$22.00
5g	97%	in stock	$90.00	$63.00
10g	97%	in stock	$155.00	$108.00
25g	97%	in stock	$298.00	$208.00
100g	97%	in stock	$1,188.00	$832.00

Description

• Catalog Number: AB57766
• Chemical Name: 1-Acenaphthenone
• CAS Number: 2235-15-6
• Molecular Formula: C12H8O
• Molecular Weight: 168.1913
• MDL Number: MFCD00156651
• SMILES: O=C1Cc2c3c1cccc3ccc2

Computed Properties

• Complexity: 233
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 1
• XLogP3: 2.6

Literature

• Ethyl (1R,1'S,2'S,7a'R)-2-oxo-1'-[(3aR,5R,5aS,8aS,8bR)-2,2,7,7-tetra-methyl-tetra-hydro-3aH-bis-[1,3]dioxolo[4,5-b:4',5'-d]pyran-5-yl]-1',2',5',6',7',7a'-hexa-hydro-2H-spiro-[acenaphthyl-ene-1,3'-pyrrolizine]-2'-carboxyl-ate.

  Acta crystallographica. Section E, Structure reports online 20120201

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

  Bioorganic & medicinal chemistry letters 20101101

• 3'-Benzoyl-1'-methyl-4'-phenyl-spiro[acenaphthyl-ene-1(2H),2'-pyrrolidin]-2-one.

  Acta crystallographica. Section E, Structure reports online 20101101

• Bacterial degradation of aromatic compounds.

  International journal of environmental research and public health 20090101

• Ethyl 3'-cyano-1'-methyl-2-oxo-4'-phenylspiro-[acenaphthene-1,2'-pyrrolidine]-3'-carboxyl-ate.

  Acta crystallographica. Section E, Structure reports online 20080201

• Metabolism of fluoranthene by Mycobacterium sp. strain AP1.

  Applied microbiology and biotechnology 20060501

• Microsphere-based protease assays and screening application for lethal factor and factor Xa.

  Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

• Degradation and formation of polycyclic aromatic compounds during bioslurry treatment of an aged gasworks soil.

  Environmental toxicology and chemistry 20030701

• New methodologies for the preparation of porphodimethenes and their conversion to trans-porphyrins with functionalized naphthyl spacers.

  The Journal of organic chemistry 20010810

• Convergent and divergent points in catabolic pathways involved in utilization of fluoranthene, naphthalene, anthracene, and phenanthrene by Sphingomonas paucimobilis var. EPA505.

  Journal of industrial microbiology & biotechnology 20010601

• The electron as a protecting group. 3. Generation of acenaphthyne radical anion and the determination of the heat of formation of a strained cycloalkyne.

  Journal of the American Chemical Society 20010509

• Use of 13C nuclear magnetic resonance to assess fossil fuel biodegradation: fate of [1-13C]acenaphthene in creosote polycyclic aromatic compound mixtures degraded by bacteria.

  Applied and environmental microbiology 19980401