Trimethoxy(7-octen-1-yl)silane - technical grade, ≥80% , CAS No.52217-57-9

CAS: 52217-57-9 Cat. No.: T432825 Peso molecular: 232.4 Número EC: 610-800-7

GRADE & PURITY Technical grade, ≥80%

Synonyms

trimethoxy(oct-7-en-1-yl)silane | BS-49277 | MFCD00040026 | 7-Ctenyltrimethoxysilane | DTXSID7068718 | RKLXSINPXIQKIB-UHFFFAOYSA-N | CCA21757 | Trimethoxy(7-octen-1-yl)silane, >/=90% | Trimethoxy(7-Cten-1-Yl)Silane | (7-Octen-1-yl)trimethoxysilane | 7-Oct

Storage

Room temperature

Descripción general

Application

Trimethoxy(7-octen-1-yl)silane was used to silanize the surface of coverslips which were then used for DNA combing. The silane can be used as a coupling agent to link methacrylate-based polymers to a siliceous matrix.

Specifications

Sinónimos

trimethoxy(oct-7-en-1-yl)silane | BS-49277 | MFCD00040026 | 7-Ctenyltrimethoxysilane | DTXSID7068718 | RKLXSINPXIQKIB-UHFFFAOYSA-N | CCA21757 | Trimethoxy(7-octen-1-yl)silane, >/=90% | Trimethoxy(7-Cten-1-Yl)Silane | (7-Octen-1-yl)trimethoxysilane | 7-Oct

Especificaciones y pureza

technical grade, ≥80%

Condiciones de almacenamiento de almacenamiento

Room temperature

Grado

Technical grade

Pureza

≥80%

Nombres e identificadores

• Sonrisas canónicas: CO[Si](CCCCCCC=C)(OC)OC
• IUPAC Name: trimethoxy(oct-7-enyl)silane
• InChIKey: RKLXSINPXIQKIB-UHFFFAOYSA-N
• INCHI: 1S/C11H24O3Si/c1-5-6-7-8-9-10-11-15(12-2,13-3)14-4/h5H,1,6-11H2,2-4H3
• Isómeros SMILES: CO[Si](CCCCCCC=C)(OC)OC
• Peso molecular: 232.4

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Clase Organometalloid compounds
      • Subclass Organosilicon compounds
        • Level5 Alkoxysilanes
          • Level6 Trialkoxysilanes

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Clase: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Alkoxysilanes
• Direct Parent: Trialkoxysilanes
• Alternative Parents: Silyl ethers Organoheterosilanes Organic metalloid salts Organooxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Trialkoxysilane - Silyl ether - Organoheterosilane - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as trialkoxysilanes. These are organosilicon compounds with the general formula RO[Si](R')(OR'')OR''' (R-R''' = aliphatic organyl 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

Propiedades químicas y físicas

• Punto de inflamación (°C): 94°C
• Punto de ebullición (°C): 49°C/0.1mmHg
• Peso molecular: 232.390 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 10
• Exact Mass: 232.149 Da
• Monoisotopic Mass: 232.149 Da
• Topological Polar Surface Area: 27.700 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 150.000
• 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

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