Acido DL-3-fenilattico - ≥98% , CAS No.828-01-3

CAS: 828-01-3 Cat. No.: P113801 Formula: C₉H₁₀O₃ Peso molecolare: 166.17 Beilstein Registry Number: 2209791 Numero EC: 212-580-4

GRADE & PURITY ≥98%

Synonyms

3-Phenyl-2-hydroxypropanoate | 8C1DB5C8-C19C-4963-8F3E-B683EAB4B04F | DL-b-Phenyllactic acid | Lactic acid, 3-phenyl-, DL- | beta-Phenyllactic acid | AC1610 | AI3-50440 | DL-Phenyllactic acid | DL--Phenyllactic acid | FT-0624395 | SC6T4O59BK | SCHEMBL5755

Storage

Room temperature

Shipped In

Normale

Specifications

Sinonimi

3-Phenyl-2-hydroxypropanoate | 8C1DB5C8-C19C-4963-8F3E-B683EAB4B04F | DL-b-Phenyllactic acid | Lactic acid, 3-phenyl-, DL- | beta-Phenyllactic acid | AC1610 | AI3-50440 | DL-Phenyllactic acid | DL--Phenyllactic acid | FT-0624395 | SC6T4O59BK | SCHEMBL5755

Specifiche e purezza

≥98%

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normale

Tipo di azione

INHIBITOR

Purezza

≥98%

Nomi e identificatori

• Pubchem Sid: 488179802
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488179802
• Sorrisi canonici: C1=CC=C(C=C1)CC(C(=O)O)O
• IUPAC Name: 2-hydroxy-3-phenylpropanoic acid
• InChIKey: VOXXWSYKYCBWHO-UHFFFAOYSA-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)
• Isomeri SMILES: C1=CC=C(C=C1)CC(C(=O)O)O
• WGK Germania: 3
• Peso molecolare: 166.17
• Beilstein: 2209791
• 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
    • Classe Phenylpropanoic acids

• Kingdom: Organic compounds
• Superclass: Phenylpropanoids and polyketides
• Classe: 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
• Descrizione: 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: 2-hydroxy monocarboxylic 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

Obiettivi associati (umani)

Jurkat (10389 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Obiettivi associati (non umani)

blaZ Beta-lactamase (285 Activities)

Discover Target: blaZ

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Punto di fusione (°C): 95-98°C
• Peso molecolare: 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: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Riferimenti

1. Qiuyang Huang, Xiaoling Zang, Zhiwei Zhang, Hang Yu, Baoyan Ding, Zhuangzhuang Li, Simin Cheng, Xin Zhang, Mustafa R.K. Ali, Xue Qiu, Zhihua Lv.  (2023)  Study on endogenous inhibitors against PD-L1: cAMP as a potential candidate.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:36646351] [10.1016/j.ijbiomac.2023.123266]

2. Cheng Wang, Hao Yu, QiHang Bu, ZiHan Wang, Ning Jiang, JiaoYang Chen, RongXue Sun, QianYuan Liu, JianHua Xu, JiaJun Fu.  (2025)  Supramolecular interaction-enhanced green active packaging films: Design and performance of Ca2+-crosslinked carboxymethyl chitosan composite films.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:40210045] [10.1016/j.ijbiomac.2025.143002]

3. Dongqing Li, Zhaohui Chen, En Zhao, Yanmei Zheng, Lin Dong, Wenjun Zhang, Zupeng Chen.  (2025)  Efficient photocatalytic conversion of biomass-derived hydroxyl acids to amino acids over Ni/CdS.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:41240565] [10.1016/j.jcis.2025.139400]