Reagente Nysted - sospensione al 20 % in peso in THF , CAS No.41114-59-4

CAS: 41114-59-4 Cat. No.: N124096 Formula: C₆H₁₂Br₂OZn₃ Peso molecolare: 456.14

GRADE & PURITY 20 wt. % suspension in THF

Synonyms

DTXSID1061071 | EINECS 212-042-9 | AMY1250 | (trimethylsilyl)ethene | V0067 | Vinyltrimethylsilane, >=99.5% | MFCD00008606 | NSC 93553 | BP-21122 | NSC-115430 | C.I. Disperse Blue 73 | NSC93553 | NSC-93553 | hydroxyisocaproic acid | J-525108 | A851124 | N

Storage

Argon charged,Room temperature

Shipped In

Normale

Panoramica

Reagente per:

- Sintesi dell'anfidinolide T3 mediante metatesi ad anello e diidrossilazione asimmetrica

- Metilazione di composti carbonilici

- Reazioni di olefinazione

Reagente utile per la metilazione di chetoni e α-chetoli.

Specifications

Sinonimi

DTXSID1061071 | EINECS 212-042-9 | AMY1250 | (trimethylsilyl)ethene | V0067 | Vinyltrimethylsilane, >=99.5% | MFCD00008606 | NSC 93553 | BP-21122 | NSC-115430 | C.I. Disperse Blue 73 | NSC93553 | NSC-93553 | hydroxyisocaproic acid | J-525108 | A851124 | N

Specifiche e purezza

sospensione al 20 % in peso in THF

Condizioni di conservazione di stoccaggio

Argon charged,Room temperature

Spedito in

Normale

Nomi e identificatori

Pubchem Sid

508811003

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508811003

Sorrisi canonici

C[Si](C)(C)C=C

IUPAC Name

ethenyl(trimethyl)silane

InChIKey

GCSJLQSCSDMKTP-UHFFFAOYSA-N

INCHI

1S/C5H12Si/c1-5-6(2,3)4/h5H,1H2,2-4H3

Isomeri SMILES

C[Si](C)(C)C=C

WGK Germania

3

CAS alternativo

41114-59-4

Peso molecolare

456.14

Reaxy-Rn

956572

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=956572&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Classe Organometalloid compounds
      • Subclass Organosilicon compounds
        • Level5 Alkylsilanes
          • Level6 Trialkylsilanes

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Classe: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Alkylsilanes
• Direct Parent: Trialkylsilanes
• Alternative Parents: Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Trialkylsilane - Hydrocarbon derivative - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as trialkylsilanes. These are organosilicon compounds containing exactly one alkyl chain attached to the silicon 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

Proprietà chimiche e fisiche

• Sensibilità: Air & Moisture Sensitive
• Punto di infiammabilità (°F): -14.8 °F
• Punto di infiammabilità (°C): -26°C
• Peso molecolare: 100.230 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 100.071 Da
• Monoisotopic Mass: 100.071 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 49.400
• 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