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(Triethylsilyl)acetylene 三乙基硅基乙炔

规格: 97%
CAS: 1777-03-3
产品编号: H29614
MDL: MFCD00075373
品牌: INFI
Chemical Name(Triethylsilyl)acetylene
CAS Number1777-03-3
EC Number000-000-0
Beilstein Registry Number4(4)3937
MDL NumberMFCD00075373
Synonym Triethyl(ethynyl)silane
PubChem Substance ID87559133
Chemical Name Translation三乙基硅基乙炔
Reaxys-RN1743814
LabNetwork Molecule IDLN00010289
Canonical SMILESC#C[Si](CC)(CC)CC
IUPAC Nametriethyl(ethynyl)silane
  • (Triethylsilyl)acetylene may be used in the synthesis of triethylsilylethynyl anthradithiophenes, such as :
  • · 2,8-dimethyl-5,11-bis(triethylsilylethynyl)ADT (ADT= anthradithiophene);
  • · 2,8-diethyl-5,11-bis(triethylsilylethynyl)ADT;
  • · 2,8-dipropyl-5,11-bis(triethylsilylethynyl)ADT.
  • {ALD} Beilstein:4(4)3937
  • {PUB} PubChem --- Efficient Preparation of Photoswitchable Dithienylethene‐Linker‐Conjugates by Palladium‐Catalyzed Coupling Reactions of Terminal Alkynes with Thienyl Chlorides and Other Aryl Halides --- https://pubmed.ncbi.nlm.nih.gov/20340153
  • {PUB} PubChem --- Total Synthesis of (S)-(−)-(E)-15,16-Dihydrominquartynoic Acid: A Highly Potent Anticancer Agent --- https://pubmed.ncbi.nlm.nih.gov/15132560
  • {PUB} PubChem --- Transient and Switchable (Triethylsilyl)ethynyl Protection of DNA against Cleavage by Restriction Endonucleases --- https://pubmed.ncbi.nlm.nih.gov/21805545
  • {PUB} PubChem|Springer Nature --- Synthesis of Nucleobase-Functionalized Morpholino Monomers --- https://pubmed.ncbi.nlm.nih.gov/31016698
  • {PUB} PubChem|The Cambridge Structural Database --- Stereochemical and Skeletal Diversity Arising from Amino Propargylic Alcohols --- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883853
  • {PUB} Springer Nature --- 1-(2′-triethylsilylethyl)-, 1-(2′-triethylsilylvinyl)-, and 1′-(2′-triethylsilylethynyl)-silatranes --- https://doi.org/10.1007/bf00948861
  • {PUB} Springer Nature --- Applications of metal and non-metal catalysts for the synthesis of oxygen containing five-membered polyheterocylces: a mini review --- https://doi.org/10.1007/s42452-019-1007-1
  • {PUB} Springer Nature --- Bimetallic derivatives of ethylene --- https://doi.org/10.1007/bf01176046
  • {PUB} Springer Nature --- Copper(I)-Halide-Catalyzed Oxidative Coupling of Acetylenes --- https://doi.org/10.1007/978-3-642-60328-0_5
  • {PUB} Springer Nature --- Cu/Pd-catalyzed borocarbonylative trifunctionalization of alkynes and allenes: synthesis of β-geminal-diboryl ketones --- https://doi.org/10.1007/s11426-021-1054-4
  • {PUB} Springer Nature --- Effect of viscosity on separation of carbon isotopes during photolysis of dibenzyl ketone --- https://doi.org/10.1007/bf00952400
  • {PUB} Springer Nature --- Hydrosilylation of Alkynes and Their Derivatives --- https://doi.org/10.1007/978-1-4
  • 1777-03-3 H29614 (Triethylsilyl)acetylene
三乙基硅基乙炔

    化学属性

    Mol. FormulaC8H16Si
    Mol. Weight140.30
    Density0.763
    Refractive index1.4290 to 1.4330
    Flash Point17 °C - 闭杯
    TSCANo
    Boiling Point140.2°C at 760 mmHg
    Stability对湿度和空气敏感
    Melting Point95-97 °C

    *以上化合物性质及应用等信息仅供参考