591-24-2 | 3-Methylcyclohexanone

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$26.00	$18.00
5g	95%	in stock	$34.00	$24.00
25g	95%	in stock	$74.00	$52.00
100g	95%	in stock	$203.00	$142.00

Description

• Catalog Number: AB65368
• Chemical Name: 3-Methylcyclohexanone
• CAS Number: 591-24-2
• Molecular Formula: C7H12O
• Molecular Weight: 112.1696
• MDL Number: MFCD00001639
• SMILES: CC1CCCC(=O)C1
• NSC Number: 3709

Computed Properties

• Complexity: 96.6
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 1
• Undefined Atom Stereocenter Count: 1
• XLogP3: 1.4

Literature

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  Chemical communications (Cambridge, England) 20120904

• Probing enantioselectivity on chirally modified Cu(110), Cu(100), and Cu(111) surfaces.

  Langmuir : the ACS journal of surfaces and colloids 20101102

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

  Bioorganic & medicinal chemistry letters 20101101

• Asymmetric total syntheses of cyclic nitrone-containing phlegmarine-type Lycopodium alkaloids, lycoposerramines-X and -Z.

  The Journal of organic chemistry 20091120

• Enaminones 10. Molecular modeling aspects of the 5-methylcyclohexenone derivatives.

  Bioorganic & medicinal chemistry 20090715

• Synthetic studies of the zoanthamine alkaloids: the total syntheses of norzoanthamine and zoanthamine.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20090706

• Total synthesis of grandisine D.

  Organic letters 20090305

• Total synthesis of (+)-neomarinone.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20090101

• Nitration versus nitrosation chemistry of menthofuran: remarkable fragmentation and dimerization pathways and expeditious entry into dehydromenthofurolactone.

  The Journal of organic chemistry 20071221

• Stepwise acid-promoted double-Michael process: an alternative to Diels-Alder cycloadditions for hindered silyloxydiene-dienophile pairs.

  Organic letters 20070118

• Do alpha-acyloxy and alpha-alkoxycarbonyloxy radicals fragment to form acyl and alkoxycarbonyl radicals?

  Beilstein journal of organic chemistry 20060101

• Enolate structure and electron affinity.

  The journal of physical chemistry. A 20051006

• Enantioselective separation on a naturally chiral surface.

  Journal of the American Chemical Society 20041117

• Tetrahydroacridin-9-ones, 9-chlorotetrahydroacridines, 9-amino-tetrahydroacridines and 9-(pyrazol-1-yl)-tetrahydroacridines derived from chiral cyclanones.

  European journal of medicinal chemistry 20040101

• Enantiospecific desorption of chiral compounds from chiral Cu(643) and achiral Cu(111) surfaces.

  Journal of the American Chemical Society 20020313