Ethyltriacetoxysilane - ≥96% , CAS No.17689-77-9

CAS: 17689-77-9 Cat. No.: E124668 Fórmula: C₈H₁₄O₆Si Peso molecular: 234.28 Beilstein Registry Number: 1795013 Número CE: 241-677-4

GRADE & PURITY ≥96%

Synonyms

ChemDiv2_002403 | NCGC00249090-01 | Ethyltriacethoxysilane | Silanetriol, ethyl-, triacetate | SCHEMBL131295 | [diacetyloxy(ethyl)silyl] acetate | 2-Amino-3-cyano-4,5-hexamethylenethiophene | MFCD00053703 | TRIS(ACETYLOXY)ETHYLSILANE | J-502569 | NCGC0025

Storage

Room temperature,Argon charged,Desiccated

Shipped In

Normal

Visão geral

Application：

Triacetoxy(ethyl)silane is used in sealants, the substance is used as a cross-linking agent and adhesion promoter.

Specifications

Sinónimos

ChemDiv2_002403 | NCGC00249090-01 | Ethyltriacethoxysilane | Silanetriol, ethyl-, triacetate | SCHEMBL131295 | [diacetyloxy(ethyl)silyl] acetate | 2-Amino-3-cyano-4,5-hexamethylenethiophene | MFCD00053703 | TRIS(ACETYLOXY)ETHYLSILANE | J-502569 | NCGC0025

Especificações e pureza

≥96%

Condições de armazenamento de armazenamento

Room temperature,Argon charged,Desiccated

Enviado em

Normal

Pureza

≥96%

Nomes e identificadores

• Pubchem Sid: 528769344
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/528769344
• Sorrisos canónicos: CC[Si](OC(=O)C)(OC(=O)C)OC(=O)C
• IUPAC Name: [diacetyloxy(ethyl)silyl] acetate
• InChIKey: KXJLGCBCRCSXQF-UHFFFAOYSA-N
• INCHI: 1S/C8H14O6Si/c1-5-15(12-6(2)9,13-7(3)10)14-8(4)11/h5H2,1-4H3
• SMILES isoméricas: CC[Si](OC(=O)C)(OC(=O)C)OC(=O)C
• WGK Alemanha: 3
• Peso molecular: 234.28
• Beilstein: 1795013
• Reaxy-Rn: 1795013
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1795013&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Tricarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Tricarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Tricarboxylic acids and derivatives
• Alternative Parents: Trialkoxysilanes Acetate salts Organoheterosilanes Organic metalloid salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tricarboxylic acid or derivatives - Trialkoxysilane - Acetate salt - Alkoxysilane - Carboxylic acid salt - Organoheterosilane - Organic metalloid salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organosilicon compound - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.
• 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

Propriedades químicas e físicas

• Sensibilidade: Moisture Sensitive
• Índice de refração: 1.412
• Ponto de inflamação (°F): 224°F
• Ponto de inflamação (°C): 106°C
• Ponto de ebulição (°C): 109°C/10mmHg
• Ponto de fusão (°C): 7-9°C
• Peso molecular: 234.280 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 7
• Exact Mass: 234.056 Da
• Monoisotopic Mass: 234.056 Da
• Topological Polar Surface Area: 78.900 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 234.000
• 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

Referências

1. Yingpeng Huo, Jiwen Hu, Yuanyuan Tu, Zhenzhu Huang, Shudong Lin, Yangfei Hu, Chao Feng.  (2020)  Platinum-Imidazolyl Schiff Base Complexes Immobilized in Periodic Mesoporous Organosilica Frameworks as Catalysts for Hydrosilylation.  APPLIED ORGANOMETALLIC CHEMISTRY,  34  (8): (e5697).  [PMID:] [10.1002/aoc.5697]