(Chloromethyl)trimethylsilane - ≥98% , CAS No.2344-80-1

CAS: 2344-80-1 Cat. No.: C115785 Molecular Weight: 122.67 Beilstein Registry Number: 906705 EC Number: 219-058-5

GRADE & PURITY ≥98%

Synonyms

trimethylchloromethylsilane | Chloromethyl trimethylsilane | Chloromethyltrimethylsilane | chloromethyl-trimethylsilane | chloromethyltrimethyl-silane | S04425 | CC3285 | AKOS000121082 | Silane, (chloromethyl)trimethyl- | DTXSID7020053 | DTXSID9046653 | E

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Specifications

Synonyms

trimethylchloromethylsilane | Chloromethyl trimethylsilane | Chloromethyltrimethylsilane | chloromethyl-trimethylsilane | chloromethyltrimethyl-silane | S04425 | CC3285 | AKOS000121082 | Silane, (chloromethyl)trimethyl- | DTXSID7020053 | DTXSID9046653 | E

Specifications & Purity

≥98%

Storage

Room temperature, Argon charged

Shipped In

FedEx DG Service

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 504754936
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754936
• Canonical Smiles: C[Si](C)(C)CCl
• IUPAC Name: chloromethyl(trimethyl)silane
• InChIKey: OOCUOKHIVGWCTJ-UHFFFAOYSA-N
• INCHI: 1S/C4H11ClSi/c1-6(2,3)4-5/h4H2,1-3H3
• Isomeric SMILES: C[Si](C)(C)CCl
• WGK Germany: 3
• UN Number: 2924
• Packing Group: II
• Molecular Weight: 122.67
• Beilstein: 906705
• Reaxy-Rn: 906705
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=906705&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic salts
    • Class Organic metal salts
      • Subclass Organic metalloid salts

• Kingdom: Organic compounds
• Superclass: Organic salts
• Class: Organic metal salts
• Subclass: Organic metalloid salts
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic metalloid salts
• Alternative Parents: Organochlorides Hydrocarbon derivatives Alkylsilanes Alkyl chlorides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organic metalloid salt - Hydrocarbon derivative - Organosilicon compound - Alkylsilane - Organochloride - Organohalogen compound - Alkyl halide - Alkyl chloride - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as organic metalloid salts. These are organic salt compounds containing a metalloid atom in its ionic form.
• 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

Chemical and Physical Properties

• Solubility: Soluble in water (0.4g/L at 20°C).
• Sensitivity: Moisture sensitive.
• Refractive Index: 1.42
• Flash Point(°F): 24.8 °F
• Flash Point(°C): -4 °C
• Boil Point(°C): 98-99°C
• Molecular Weight: 122.670 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 122.032 Da
• Monoisotopic Mass: 122.032 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 37.300
• 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

References

1. Bo Hao, Wenbo Zhao, Xiangxin Tong, Shaoyun Shan, Yuan Chen.  (2022)  Low viscous aminoalkyl-phenyl-silane with π–π interaction and its optimal SO2 capture condition.  AICHE JOURNAL,  68  (10): (e17775).  [PMID:] [10.1002/aic.17775]

2. Bo Hao, Wenbo Zhao, Dong Feng, Shengchao Xu, Yuan Chen.  (2020)  Synthesis of dibutyl-trimethylsilanylmethyl-amine and its application towards SO2 absorption with phase change behaviors.  NEW JOURNAL OF CHEMISTRY,  44  (48): (21228-21237).  [PMID:] [10.1039/D0NJ04500D]