5267-64-1 | D-Phenylalaninol

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$6.00	$4.00
5g	98%	in stock	$8.00	$6.00
10g	98%	in stock	$10.00	$7.00
25g	98%	in stock	$22.00	$16.00
100g	98%	in stock	$87.00	$61.00
500g	98%	in stock	$395.00	$276.00

Description

• Catalog Number: AB42750
• Chemical Name: D-Phenylalaninol
• CAS Number: 5267-64-1
• Molecular Formula: C9H13NO
• Molecular Weight: 151.2056
• MDL Number: MFCD00064298
• SMILES: OC[C@@H](Cc1ccccc1)N

Computed Properties

• Complexity: 99.7
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• XLogP3: 0.7

Upstream Synthesis Route

In chemical synthesis, (+)-D-Phenylalaninol is a valuable chiral building block known for its ability to impart optical activity to synthesized compounds. With its unique stereochemistry, this compound serves as a key intermediate in the development of various pharmaceuticals, agrochemicals, and fine chemicals. Its presence can influence the stereoselectivity and overall efficiency of synthetic pathways, making it a versatile tool for controlling the chirality of target molecules. Researchers and chemists utilize (+)-D-Phenylalaninol as a catalyst or precursor in asymmetric synthesis reactions, enabling the production of enantiomerically pure compounds with high levels of optical purity. This compound plays a crucial role in the development of complex molecules with specific biological or chemical properties, highlighting its importance as a valuable component in modern synthetic chemistry.

Literature

• A colorimetric chiral sensor based on chiral crown ether for the recognition of the two enantiomers of primary amino alcohols and amines.

  Chirality 20110401

• Direct high-performance liquid chromatographic separation of the enantiomers of an aromatic amine and four aminoalcohols using polysaccharide chiral stationary phases and acidic additive.

  Chirality 20070801

• Straightforward methodology for the enantioselective synthesis of benzo[a]- and indolo[2,3-a]quinolizidines.

  The Journal of organic chemistry 20070706

• Structural and mechanistic insights into polyketide macrolactonization from polyketide-based affinity labels.

  Nature chemical biology 20061001

• Synthesis and activity of 2-oxoamides containing long chain beta-amino acids.

  Journal of peptide science : an official publication of the European Peptide Society 20050701

• Chiral bis(amino alcohol)oxalamide gelators-gelation properties and supramolecular organization: racemate versus pure enantiomer gelation.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20031121

• Chemotactic peptide analogues. Synthesis and chemotactic activity of N-formyl-Met-Leu-Phe analogues containing (S)-phenylalaninol derivatives.

  Archiv der Pharmazie 19950901