Methyltrichlorosilane - ≥98% , CAS No.75-79-6

CAS: 75-79-6 Cat. No.: M414615 Formula: CH₃SiCl₃ Peso molecolare: 149.48 Numero EC: 200-902-6

GRADE & PURITY ≥98%

Synonyms

Methylsilyl trichloride | Methylsilicochloroform | Methyl-trichlorsilan | Trichloro(methyl)silane | Trichloromethylsilane | Monomethyltrichlorosilane | Silane, trichloromethyl- | METHYLTRICHLOROSILANE | Trichloromethylsilicon

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Panoramica

application：

Methyltrichlorosilane (MTS) can be used:

As a reagent for the surface-functionalization of fabrics and mesoporous materials to increase their hydrophobicity.

As a source of silicon to synthesize silica doped carbon nanotubes.

Specifications

Sinonimi

Methylsilyl trichloride | Methylsilicochloroform | Methyl-trichlorsilan | Trichloro(methyl)silane | Trichloromethylsilane | Monomethyltrichlorosilane | Silane, trichloromethyl- | METHYLTRICHLOROSILANE | Trichloromethylsilicon

Specifiche e purezza

≥98%

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged

Spedito in

FedEx DG Service

Purezza

≥98%

Nomi e identificatori

Pubchem Sid

508814835

Sorrisi canonici

C[Si](Cl)(Cl)Cl

IUPAC Name

trichloro(methyl)silane

InChIKey

JLUFWMXJHAVVNN-UHFFFAOYSA-N

INCHI

1S/CH3Cl3Si/c1-5(2,3)4/h1H3

Isomeri SMILES

C[Si](Cl)(Cl)Cl

Numero UN

1250

Gruppo di imballaggio

II

Peso molecolare

149.48

Reaxy-Rn

1361381

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1361381&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Classe Organometalloid compounds
      • Subclass Organosilicon compounds
        • Level5 Organoheterosilanes
          • Level6 Organochlorosilanes

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Classe: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Organoheterosilanes
• Direct Parent: Organochlorosilanes
• Alternative Parents: Organic metalloid salts Alkylhalosilanes Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organochlorosilane - Organic metalloid salt - Alkylhalosilane - Hydrocarbon derivative - Organic salt - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as organochlorosilanes. These are organosilicon compounds where the tetravalent silicon atom is linked to one or more chlorine atoms.
• 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

• Solubilità: Reacts with water
• Sensibilità: Moisture & Light sensitive.
• Indice di rifrazione: 1.4085
• Punto di infiammabilità (°C): 8°F
• Punto di ebollizione (°C): 66.4°C
• Punto di fusione (°C): -90°C(lit.)
• Peso molecolare: 149.470 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 147.907 Da
• Monoisotopic Mass: 147.907 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 28.400
• 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