6859-99-0 | Piperidin-3-ol

Packsize	Purity	Availability	Price	Discounted Price
10g	98%	in stock	$11.00	$8.00
25g	98%	in stock	$21.00	$15.00
500g	98%	in stock	$297.00	$208.00

Description

• Catalog Number: AB44600
• Chemical Name: Piperidin-3-ol
• CAS Number: 6859-99-0
• Molecular Formula: C5H11NO
• Molecular Weight: 101.1469
• MDL Number: MFCD00014591
• SMILES: OC1CCCNC1
• NSC Number: 62082

Computed Properties

• Complexity: 56
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Undefined Atom Stereocenter Count: 1
• XLogP3: -0.3

Literature

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  Clinical pharmacokinetics 20120701

• Facile syntheses of enantiopure 3-hydroxypiperidine derivatives and 3-hydroxypipecolic acids.

  The Journal of organic chemistry 20100305

• Dihydroxylation of vinyl sulfones: stereoselective synthesis of (+)- and (-)-febrifugine and halofuginone.

  The Journal of organic chemistry 20100115

• A concise and fully selective synthesis of the ant venom alkaloid (3S,5R,8S,9S)-3-butyl-5-propyl-8-hydroxyindolizidine.

  Organic & biomolecular chemistry 20091107

• Complementary chemoenzymatic routes to both enantiomers of febrifugine.

  Organic & biomolecular chemistry 20090721

• Asymmetric synthesis of (+)-isofebrifugine and (-)-sedacryptine from a common chiral nonracemic building block.

  Organic letters 20080904

• Application of the aza-Achmatowicz oxidative rearrangement for the stereoselective synthesis of the Cassia and Prosopis alkaloid family.

  The Journal of organic chemistry 20061027

• Methods for the synthesis of polyhydroxylated piperidines by diastereoselective dihydroxylation: exploitation in the two-directional synthesis of aza-C-linked disaccharide derivatives.

  Beilstein journal of organic chemistry 20050101

• An aza-Achmatowicz approach toward the hydroxylated piperidine alkaloids (+/-)-azimic acid and (+/-)-deoxocassine.

  Organic letters 20041028

• Oxidation of 3-hydroxypiperidines with iodosylbenzene in water: tandem oxidative Grob fragmentation-cyclization reaction.

  Chemical & pharmaceutical bulletin 20040901

• [Synthesis and its application to the synthesis of biologically active natural products of new and versatile chiral building blocks].

  Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 20010701

• Efficient stereoselective synthesis of alpha-hydroxy aldehydes with (R)-piperidin-3-ol as a new chiral auxiliary.

  The Journal of organic chemistry 20010406