Dimethoxy(methyl)(3,3,3-trifluoropropyl)silane - ≥98%(GC) , CAS No.358-67-8

CAS: 358-67-8 Cat. No.: D155711 Molecular Weight: 202.25 Beilstein Registry Number: 1753240 EC Number: 206-619-4

GRADE & PURITY ≥98%(GC)

Synonyms

1,1,1-Trifluoro-3-[dimethoxy(methyl)silyl]propane | (3,3,3-Trifluoropropyl)methyldimethoxysilane | Dimethoxymethyl(3,3,3-trifluoropropyl)silane | dimethoxy(methyl)(3,3,3-trifluoropropyl)silane

Storage

Room temperature,Argon charged,Desiccated,Cool

Shipped In

Normal

Specifications

Synonyms

1, 1, 1-Trifluoro-3-[dimethoxy(methyl)silyl]propane | (3, 3, 3-Trifluoropropyl)methyldimethoxysilane | Dimethoxymethyl(3, 3, 3-trifluoropropyl)silane | dimethoxy(methyl)(3, 3, 3-trifluoropropyl)silane

Specifications & Purity

≥98%(GC)

Storage

Room temperature, Argon charged, Desiccated, Cool

Shipped In

Normal

Purity

≥98%(GC)

Names and Identifiers

• Pubchem Sid: 504754199
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754199
• Canonical Smiles: CO[Si](C)(CCC(F)(F)F)OC
• IUPAC Name: dimethoxy-methyl-(3,3,3-trifluoropropyl)silane
• InChIKey: DIJRHOZMLZRNLM-UHFFFAOYSA-N
• INCHI: 1S/C6H13F3O2Si/c1-10-12(3,11-2)5-4-6(7,8)9/h4-5H2,1-3H3
• Isomeric SMILES: CO[Si](C)(CCC(F)(F)F)OC
• WGK Germany: 3
• UN Number: 1993
• Packing Group: III
• Molecular Weight: 202.25
• Beilstein: 1753240
• Reaxy-Rn: 1753237
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1753237&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Class: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Not available
• Direct Parent: Alkoxysilanes
• Alternative Parents: Silyl ethers Organoheterosilanes Organic metalloid salts Organooxygen compounds Organofluorides Hydrocarbon derivatives Alkyl fluorides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alkoxysilane - Silyl ether - Organoheterosilane - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organofluoride - Organohalogen compound - Alkyl halide - Alkyl fluoride - Aliphatic acyclic compound
• Description: 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

Chemical and Physical Properties

• Sensitivity: Moisture Sensitive
• Refractive Index: 1.358
• Flash Point(°F): 134.6 °F
• Flash Point(°C): 57 °C
• Boil Point(°C): 85 °C/150 mmHg
• Molecular Weight: 202.250 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 202.064 Da
• Monoisotopic Mass: 202.064 Da
• Topological Polar Surface Area: 18.500 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 133.000
• 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

References

1. Zhen Yang, Yongping Bai, Binxiao Wei, Yutao Cui, JunHui Huang, Yingying Li, Linghui Meng, Yu Wang.  (2022)  A facile preparation method of UV rapid curing fluorosilicone coatings with good hydrophobicity and excellent corrosion resistance based on thiol-ene click reaction.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2022.107248]