1120-72-5 | 2-Methylcyclopentanone

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$8.00	$5.00
1g	97%	in stock	$13.00	$9.00
5g	97%	in stock	$27.00	$19.00
10g	97%	in stock	$49.00	$35.00
25g	97%	in stock	$92.00	$64.00
100g	97%	in stock	$280.00	$196.00

Description

• Catalog Number: AE09255
• Chemical Name: 2-Methylcyclopentanone
• CAS Number: 1120-72-5
• Molecular Formula: C6H10O
• Molecular Weight: 98.143
• MDL Number: MFCD00001414
• SMILES: O=C1CCCC1C
• NSC Number: 105429

Computed Properties

• Complexity: 86.2
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 1
• Undefined Atom Stereocenter Count: 1
• XLogP3: 1

Literature

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  Chemosphere 20120401

• (E)-2-Methyl-5-(thiophen-2-ylmethyl-idene)cyclopentan-1-one.

  Acta crystallographica. Section E, Structure reports online 20110901

• Bioreduction of α,β-unsaturated ketones and aldehydes by non-conventional yeast (NCY) whole-cells.

  Bioresource technology 20110301

• Intramolecular cyclopropene-furan [2 + 4] cycloaddition followed by a cyclopropylcarbinyl rearrangement to synthesize the BCD rings of cortistatin A.

  Organic letters 20090903

• Insights into sequence-activity relationships amongst Baeyer-Villiger monooxygenases as revealed by the intragenomic complement of enzymes from Rhodococcus jostii RHA1.

  Chembiochem : a European journal of chemical biology 20090504

• Tetranuclear BINOL-titanium complex in selective direct aldol additions.

  The Journal of organic chemistry 20080201

• Total synthesis of guanacastepene a: a route to enantiomeric control.

  The Journal of organic chemistry 20051223

• Enolate structure and electron affinity.

  The journal of physical chemistry. A 20051006

• A short and concise asymmetric synthesis of hamigeran B.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20050121

• Unfunctionalized, alpha-epimerizable nonracemic ketones and aldehydes can be accessed by crystallization-induced dynamic resolution of imines.

  Journal of the American Chemical Society 20030319

• A four-step synthesis of the hydroazulene core of guanacastepene.

  Organic letters 20010726