Fentin acetate - analytical standard , CAS No.900-95-8

CAS: 900-95-8 Cat. No.: F114816 Formule: C₂₀H₁₈SnO₂ Poids moléculaire: 409.07 Beilstein Registry Number: 4146107 Numéro CE: 212-984-0

GRADE & PURITY Analytical standard

Synonyms

B4424 | DTXCID101408 | Tinestan | Fintin acetato [Italian] | NSC 76068 | Triphenylaceto stannane | Acetato di stagno trifenile | Acetoxy-triphenyl-stannan [German] | Brestan | Trifenil stagno acetato | Weed-Hoe | Acetoxytriphenylstannane | Acetoxy-triphen

Storage

Room temperature

Shipped In

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Specifications

Synonymes

B4424 | DTXCID101408 | Tinestan | Fintin acetato [Italian] | NSC 76068 | Triphenylaceto stannane | Acetato di stagno trifenile | Acetoxy-triphenyl-stannan [German] | Brestan | Trifenil stagno acetato | Weed-Hoe | Acetoxytriphenylstannane | Acetoxy-triphen

Spécifications et pureté

analytical standard

Conditions de stockage de stockage

Room temperature

Expédié en

FedEx DG Service

Grade

Étalon d'analyse

Noms et identifiants

• Sourires canoniques: CC(=O)O[Sn](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3
• IUPAC Name: triphenylstannyl acetate
• InChIKey: WDQNIWFZKXZFAY-UHFFFAOYSA-M
• INCHI: 1S/3C6H5.C2H4O2.Sn/c3*1-2-4-6-5-3-1;1-2(3)4;/h3*1-5H;1H3,(H,3,4);/q;;;;+1/p-1
• Isomères SMILES: CC(=O)O[Sn](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3
• WGK Allemagne: 3
• RTECS: WH6650000
• Numéro ONU: 3146
• Groupe d'emballage: I
• Poids moléculaire: 409.07
• Beilstein: 4146107
• Reaxy-Rn: 3819297
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3819297&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzene and substituted derivatives
• Alternative Parents: Metal aryls Monocarboxylic acids and derivatives Carboxylic acids Organotin compounds Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Not available
• Substituents: Metal aryl - Monocyclic benzene moiety - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organotin compound - Organooxygen compound - Organometallic compound - Organic post-transition metal moeity - Carbonyl group - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
• External Descriptors: Organotin fungicides

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

Propriétés chimiques et physiques

• Poids moléculaire: 409.100 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 410.033 Da
• Monoisotopic Mass: 410.033 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 332.000
• 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

XLogP3

Références

1. Jie Xu, Tianbao Chen, Tingting Sun, Chunyang Yu, Deyue Yan, Lijuan Zhu.  (2022)  Erythrocyte membrane camouflaged siRNA/chemodrug nanoassemblies for cancer combination therapy.  Biomaterials Science,  10  (22): (6601-6613).  [PMID:36250610] [10.1039/D2BM01478E]

2. Qi Chen, Renhui Zhang, Zhongyi He, Liping Xiong.  (2021)  Tribological performance of N-containing heterocyclic triazine derivative as lubricant additive in ethylene glycol.  SURFACE AND INTERFACE ANALYSIS,  53  (12): (1027-1034).  [PMID:] [10.1002/sia.7003]

3. H. Wu, J. Peng, S. Wang, B. Xie, L. Lei, D. Zhao, H. Nie.  (2015)  Fabrication of graphene oxide-β-cyclodextrin nanoparticle releasing doxorubicin and topotecan for combination chemotherapy.  MATERIALS TECHNOLOGY,      [PMID:] [10.1179/17535557B15Y.000000004]

4. Teng-Zhou Li, Cheng-Zhuang Chen, Shao-Ying Xing, Ling Liu, Ping Li, Zhi-Hua Li.  (2024)  The Influence of Triphenyltin Exposure on the Osmoregulatory Capacity of Marine Medaka (Oryzias melastigma) at Different Salinities.  Water,  16  (7): (921).  [PMID:] [10.3390/w16070921]

5. Zheng Wang, Enhui He, Guanglei Song, Xiaohui Jiang, Liangmin Yu.  (2025)  Transparent, hydrophobic, self-polishing organosilicon-modified zinc acrylate polymer coating for marine antifouling.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2025.109143]