Dicyclopentyl(dimethoxy)silane - ≥98%(GC) , CAS No.126990-35-0

CAS: 126990-35-0 Cat. No.: D155710 Peso molecular: 228.41 Número EC: 620-337-2

GRADE & PURITY ≥98%(GC)

Synonyms

SCHEMBL24124 | AS-15387 | DTXSID80888929 | Silane, dicyclopentyldimethoxy- | A805631 | MFCD01074471 | AKOS015914599 | Cyclopentane, 1,1'-(dimethoxysilylene)bis- | BFA99035 | dicyclopentyl(dimethoxy)silane;Dicyclopentyldimethoxysilane | dicyclopentyl(dimet

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

SCHEMBL24124 | AS-15387 | DTXSID80888929 | Silane, dicyclopentyldimethoxy- | A805631 | MFCD01074471 | AKOS015914599 | Cyclopentane, 1, 1'-(dimethoxysilylene)bis- | BFA99035 | dicyclopentyl(dimethoxy)silane;Dicyclopentyldimethoxysilane | dicyclopentyl(dimet

Especificaciones y pureza

≥98%(GC)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%(GC)

Nombres e identificadores

• Pubchem Sid: 504764854
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504764854
• Sonrisas canónicas: CO[Si](C1CCCC1)(C2CCCC2)OC
• IUPAC Name: dicyclopentyl(dimethoxy)silane
• InChIKey: JWCYDYZLEAQGJJ-UHFFFAOYSA-N
• INCHI: 1S/C12H24O2Si/c1-13-15(14-2,11-7-3-4-8-11)12-9-5-6-10-12/h11-12H,3-10H2,1-2H3
• Isómeros SMILES: CO[Si](C1CCCC1)(C2CCCC2)OC
• Peso molecular: 228.41
• Reaxy-Rn: 9053256
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9053256&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Clase Organometalloid compounds
      • Subclass Organosilicon compounds

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Clase: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Not available
• Direct Parent: Alkoxysilanes
• Alternative Parents: Silyl ethers Organoheterosilanes Organic metalloid salts Organooxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: Alkoxysilane - Silyl ether - Organoheterosilane - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Aliphatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as alkoxysilanes. These are organosilicon compounds with the general formula RO[Si](OR')(R'')(R''') (R,R' = organyl; R'',R''' = any atom).
• 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

• Índice de refracción: 1.47
• Punto de inflamación (°C): 141 °C
• Punto de ebullición (°C): 120 °C/6 mmHg
• Peso molecular: 228.400 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 228.155 Da
• Monoisotopic Mass: 228.155 Da
• Topological Polar Surface Area: 18.500 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 174.000
• 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

Referencias

1. Qingtao Niu, Aihua He, Chongdian Si, Guodong Liu, Bolin Dai, Manman Jin.  (2024)  Effect of internal and external electron donors on stereospecific polymerization of isoprene with TiCl4/MgCl2 type Ziegler-Natta catalysts.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2024.113850]