D-(+)-3-Phenyllactic acid - 10mM in DMSO , CAS No.7326-19-4

CAS: 7326-19-4 Cat. No.: D425723 Summenformel: C₉H₁₀O₃ Molekulargewicht: 166.17 Beilstein Registry Number: 2209793 EG-Nummer: 230-803-3

GRADE & PURITY 10mM in DMSO

Synonyms

D-?(+)?-?Phenyllactic acid | l-2-hydroxy-3-phenyl-propionic acid | SCHEMBL180366 | (s)-a-hydroxy-benzenepropanoate | (R)-(+)-2-Hydroxy-3-phenylpropionic Acid | HY-30219 | AKOS005146076 | D/L-3-phenyllactic acid | (rac)-2-hydroxy-3-phenylpropionic acid | 3

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Übersicht

Chiral building block employed in the preparation of statine. Starting material in the preparation of the hypoglycemic agent enlitazone and of 15N-labeled phenylalanine.

Specifications

Synonyme

D-?(+)?-?Phenyllactic acid | l-2-hydroxy-3-phenyl-propionic acid | SCHEMBL180366 | (s)-a-hydroxy-benzenepropanoate | (R)-(+)-2-Hydroxy-3-phenylpropionic Acid | HY-30219 | AKOS005146076 | D/L-3-phenyllactic acid | (rac)-2-hydroxy-3-phenylpropionic acid | 3

Spezifikationen & Reinheit

10mM in DMSO

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Aktionsart

INHIBITOR

Namen und Kennungen

• Pubchem Sid: 528763978
• Kanonisches Lächeln: C1=CC=C(C=C1)CC(C(=O)O)O
• IUPAC Name: (2R)-2-hydroxy-3-phenylpropanoic acid
• InChIKey: VOXXWSYKYCBWHO-MRVPVSSYSA-N
• INCHI: 1S/C9H10O3/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8,10H,6H2,(H,11,12)/t8-/m1/s1
• Isomere SMILES: C1=CC=C(C=C1)C[C@H](C(=O)O)O
• WGK Deutschland: 3
• Molekulargewicht: 166.17
• Beilstein: 2209793
• Reaxy-Rn: 2209791
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2209791&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Phenylpropanoids and polyketides
    • Klasse Phenylpropanoic acids

• Kingdom: Organic compounds
• Superclass: Phenylpropanoids and polyketides
• Klasse: Phenylpropanoic acids
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylpropanoic acids
• Alternative Parents: Benzene and substituted derivatives Alpha hydroxy acids and derivatives Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: 3-phenylpropanoic-acid - Alpha-hydroxy acid - Monocyclic benzene moiety - Hydroxy acid - Benzenoid - Secondary alcohol - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxygen compound - Alcohol - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as phenylpropanoic acids. These are compounds with a structure containing a benzene ring conjugated to a propanoic acid.
• External Descriptors: (2R)-2-hydroxy monocarboxylic acid - 3-phenyllactic acid

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemische und physikalische Eigenschaften

• Spezifische Drehung [α]: 22° (C=2,H2O)
• Schmelzpunkt (°C): 122-124°C
• Molekulargewicht: 166.170 g/mol
• XLogP3: 1.100
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 166.063 Da
• Monoisotopic Mass: 166.063 Da
• Topological Polar Surface Area: 57.500 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 150.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referenzen

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2. Rui Cai, Linlin Gao, Yuxiang Zhang, Lu Cui, Yahong Yuan, Zhouli Wang, Tianli Yue.  (2024)  Inactivation activity and mechanism of natural antimicrobial agents against Alicyclobacillus spp. in apple juice.  FOOD CONTROL,      [PMID:] [10.1016/j.foodcont.2024.111119]

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5. Mingyang Hu, Ying He, Yunying Wang, Hongzhi Du, Liang Wang, Jie Yang, Yun Liu.  (2026)  Dual Active Sites of Metal-Free N,S-Doped Lignin-Derived Carbon Catalysts for Oxidative Esterification Depolymerization of Polyethylene Terephthalate.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.5c12502]

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7. HaoRan Jiang, Yang Qu, Qi Meng, Chenyujun Hu, Haoran Zhang, Jinqiu Tian, Bohan Xing, Bojiang Wang, Zhihao Lin, Meng Zhang, Peixun Zhang.  (2026)  Biomimetic Bamboo-Inspired Bone Repair Scaffold: Reversing Degraded States and Promoting Mesenchymal Stem Cell Differentiation.  ACS Applied Bio Materials,      [PMID:41915781] [10.1021/acsabm.6c00387]