D-(+)-3-Phenyllactic acid - Moligand™, ≥98% , CAS No.7326-19-4

CAS: 7326-19-4 Cat. No.: P102443 Peso molecular: 166.17 Beilstein Registry Number: 2209793 Número EC: 230-803-3

GRADE & PURITY Moligand™, ≥98%

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

Room temperature

Shipped In

Normal

Descripción general

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

Sinónimos

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

Especificaciones y pureza

Moligand™, ≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Grado

Moligand™

Tipo de acción

INHIBITOR

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488190957
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488190957
• Sonrisas canónicas: 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
• Isómeros SMILES: C1=CC=C(C=C1)C[C@H](C(=O)O)O
• WGK Alemania: 3
• Peso molecular: 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
    • Clase Phenylpropanoic acids

• Kingdom: Organic compounds
• Superclass: Phenylpropanoids and polyketides
• Clase: 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
• Descripción: 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

Propiedades químicas y físicas

• Solubilidad: Soluble in water
• Rotación específica [α]: 22° (C=2,H2O)
• Punto de fusión (°C): 122-124°C
• Peso molecular: 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

Referencias

1. Xiaolong Sun, Longfei Yin, Huayue Zhu, Junhao Zhu, Jiahuan Hu, Xi Luo, He Huang, Yongqian Fu.  (2022)  Enhanced Antimicrobial Cellulose/Chitosan/ZnO Biodegradable Composite Membrane.  Membranes,  12  (2): (239).  [PMID:35207160] [10.3390/membranes12020239]

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]

3. Yuan Li, Jiwei Qiu, Zhihong Liu, Huiwen Xiao, Bin Wang, Yanxi Dong, Yunong Xiao, Qi Wang, Jiali Dong, Ming Cui.  (2025)  Phytate enhances gut Parasutterella colonization to alleviate radiation injury.  Cell Chemical Biology,      [PMID:41253152] [10.1016/j.chembiol.2025.10.009]

4. Fang Ye, Zhiyi Zhang, Binghao Zhang, Xinyu Li, Jiaxi Deng, Qian Miao, Peiruo Ning, Yunlin Chi, Geng Chen, Zhangsong Wu, Qian Wang, Lezhi Xu, Ningjie Gong, Bangning Cheng, Zhigang Ma, Chungen Qian, Lizhe Zhu, Xin Pan, Yang Du.  (2025)  Structures of G-protein coupled receptor HCAR3 in complex with selective agonists reveal the basis for ligand recognition and selectivity.  PLOS BIOLOGY,  23  (12): (e3003480).  [PMID:41359625] [10.1371/journal.pbio.3003480]

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]

6. Jingfei Wang, Shuting Li, Liwu Liu, Fukai Liu, Cheng Lin, Yanju Liu, Jinsong Leng.  (2026)  4D-Printed Intelligent Reconfigurable Occluder With Anti-Thrombotic and Rapid-Repairing Capabilities for Patent Foramen Ovale.  Advanced Healthcare Materials,      [PMID:41645865] [10.1002/adhm.202505214]

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:] [10.1021/acsabm.6c00387]