611-71-2 | (R)-(-)-Mandelic acid

Packsize	Purity	Availability	Price	Discounted Price
10g	97%	in stock	$6.00	$4.00
25g	97%	in stock	$8.00	$5.00
100g	97%	in stock	$16.00	$11.00
500g	97%	in stock	$42.00	$30.00

Description

• Catalog Number: AB42853
• Chemical Name: (R)-(-)-Mandelic acid
• CAS Number: 611-71-2
• Molecular Formula: C8H8O3
• Molecular Weight: 152.1473
• MDL Number: MFCD00064251
• SMILES: O[C@H](c1ccccc1)C(=O)O

Computed Properties

• Complexity: 138
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2
• XLogP3: 0.6

Literature

• Investigating chiral recognizability of diastereomeric crystallization of mandelic acid and L-phenylalanine.

  Journal of nanoscience and nanotechnology 20120901

• Feasibility of Repurposing the Polyanionic Microbicide, PPCM, for Prophylaxis against HIV Transmission during ART.

  ISRN obstetrics and gynecology 20110101

• Metabolic engineering of the L-phenylalanine pathway in Escherichia coli for the production of S- or R-mandelic acid.

  Microbial cell factories 20110101

• Enantiomer separation of alpha-hydroxy acids in high-performance immunoaffinity chromatography.

  Journal of pharmaceutical and biomedical analysis 20080414

• Anti-HIV-1 activity of poly(mandelic acid) derivatives.

  Biomacromolecules 20071101

• Intermediate analogue inhibitors of mandelate racemase: N-Hydroxyformanilide and cupferron.

  Bioorganic & medicinal chemistry letters 20070101

• Perturbing the hydrophobic pocket of mandelate racemase to probe phenyl motion during catalysis.

  Biochemistry 20050628

• The first preparation of enantiopure 1-methyl-7-oxabicyclo[2.2.1]heptan-2-one, a versatile chiral building block for terpenoids.

  Chirality 20050201

• Inhibition of mandelate racemase by alpha-fluorobenzylphosphonates.

  Bioorganic & medicinal chemistry letters 20030616

• Structural and kinetic analysis of catalysis by a thiamin diphosphate-dependent enzyme, benzoylformate decarboxylase.

  Biochemistry 20030225

• alpha-Ketocarboxylic acid-based inhibitors of protein tyrosine phosphatases.

  Bioorganic & medicinal chemistry letters 20010723