acido 4-etilbenzoico - ≥98% , CAS No.619-64-7

CAS: 619-64-7 Cat. No.: E156333 Formula: C₉H₁₀O₂ Peso molecolare: 150.18 Numero EC: 210-605-3

GRADE & PURITY ≥98%

Synonyms

ZQVKTHRQIXSMGY-UHFFFAOYSA- | 4-Ethyl Benzoic acid | AE-641/00011036 | MLS000849800 | 4-Ethylbenzoic acid, 99% | NCGC00246660-01 | STL168364 | SB66834 | NSC59888 | NSC-59888 | p-Ethylbenzoic acid | W-105068 | E0379 | DTXSID3073212 | Z104478474 | SMR0004558

Storage

Room temperature

Shipped In

Normale

Panoramica

l'acido 4-etilbenzoico reagisce con il nitrato di lantanio in soluzione acquosa per produrre il polimero catena-polyaqua(acido 4-etilbenzoico-κO)lantanio(III)-tri-μ-4-etilbenzoato.
l'acido 4-etilbenzoico è stato utilizzato per la sintesi dell'etil 4-vinil-α-ciano-β-fenilcinnamato. È stato inoltre utilizzato per funzionalizzare il bordo della grafite "incontaminata" in presenza di acido polifosforico/ pentossido di fosforo.

Specifications

Sinonimi

ZQVKTHRQIXSMGY-UHFFFAOYSA- | 4-Ethyl Benzoic acid | AE-641/00011036 | MLS000849800 | 4-Ethylbenzoic acid, 99% | NCGC00246660-01 | STL168364 | SB66834 | NSC59888 | NSC-59888 | p-Ethylbenzoic acid | W-105068 | E0379 | DTXSID3073212 | Z104478474 | SMR0004558

Specifiche e purezza

≥98%

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normale

Purezza

≥98%

Nomi e identificatori

• Pubchem Sid: 488181539
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181539
• Sorrisi canonici: CCC1=CC=C(C=C1)C(=O)O
• IUPAC Name: 4-ethylbenzoic acid
• InChIKey: ZQVKTHRQIXSMGY-UHFFFAOYSA-N
• INCHI: 1S/C9H10O2/c1-2-7-3-5-8(6-4-7)9(10)11/h3-6H,2H2,1H3,(H,10,11)
• Isomeri SMILES: CCC1=CC=C(C=C1)C(=O)O
• WGK Germania: 3
• Peso molecolare: 150.18
• Reaxy-Rn: 2041840
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2041840&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Benzoic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Benzoic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzoic acids
• Alternative Parents: Benzoyl derivatives Monocarboxylic acids and derivatives Carboxylic acids Organooxygen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Benzoic acid - Benzoyl - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as benzoic acids. These are organic Compounds containing a benzene ring which bears at least one carboxyl group.
• External Descriptors: Not available

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)

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

Discover Target: ALDH1A1

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Solubility in Methanol almost transparency
• Punto di fusione (°C): 113℃
• Peso molecolare: 150.170 g/mol
• XLogP3: 2.900
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 150.068 Da
• Monoisotopic Mass: 150.068 Da
• Topological Polar Surface Area: 37.300 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 134.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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

Riferimenti

1. Di Liu, Jiulong Yin, Hai Tang, Hui Wang, Shasha Liu, Tingting Huang, Sisheng Fang, Kaixuan Zhu, Zongli Xie.  (2021)  Fabrication of ZIF-67@PVDF ultrafiltration membrane with improved antifouling and separation performance for dye wastewater treatment via sulfate radical enhancement.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2021.119755]

2. Xiaoya Guo, Zhiyu Yang, Zhaopei Guo, Huiyan Lai, Hanyu Meng, Meng Meng, Tong Li, Zhen Li, Jie Chen, Yuanji Feng, Xuan Pang, Huayu Tian, Xuesi Chen.  (2025)  A Polymeric mRNA Vaccine Featuring Enhanced Site-Specific mRNA Delivery and Inherent STING-Stimulating Performance for Tumor Immunotherapy.  ADVANCED MATERIALS,      [PMID:40095378] [10.1002/adma.202410998]