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(S)-methyl 3-methyl-2-(methyl(2'-(2-trityl-2H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)amino)butanoate

(S)-methyl 3-methyl-2-(methyl(2'-(2-trityl-2H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)amino)butanoate

6,13-bis((triisopropylsilyl)ethynyl)pentacene

$200.00
CAS No.: 373596-08-8
Catalog No.: LT0278
Purity: 95%
MF: C44H54Si2
MW: 639.088
Storage: 2-8 degree Celsius
SMILES: C(C)(C)[Si](C(C)C)(C(C)C)C#CC1=C2C=C3C=CC=CC3=CC2=C(C2=CC3=CC=CC=C3C=C12)C#C[Si](C(C)C)(C(C)C)C(C)C
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CAS NO.: 373596-08-8;6,13-bis((triisopropylsilyl)ethynyl)pentacene. PROPERTIES: This silyl-protected pentacene derivative presents as a dark blue solid with a molecular weight of approximately 538.7 g/mol. The 6,13-bis((triisopropylsilyl)ethynyl)pentacene combines a pentacene backbone with two ethynyltriisopropylsilyl groups. It exhibits limited solubility in common organic solvents but dissolves in chlorobenzene and o-dichlorobenzene. Stability characterization reveals sensitivity to atmospheric moisture and oxygen, necessitating storage at 2-8 degree Celsius under inert atmosphere in sealed glass containers. Handlers should employ full-face respirators and use PTFE-lined transfer devices. Skin absorption may cause systemic toxicity requiring immediate medical attention. Inhalation poses risk of pulmonary fibrosis; treatment includes corticosteroid therapy. Eye contact requires 15 minutes of rinsing followed by ophthalmology consultation. Waste should be processed through activated carbon prior to disposal. APPLICATIONS: The 6,13-bis((triisopropylsilyl)ethynyl)pentacene serves as a key intermediate in organic electronics and specialty materials. Its silyl-protected ethynyl groups provide handles for chemical functionalization and improved solubility. Research teams utilize this compound for creating solution-processable organic semiconductors. The ethynyl groups undergo click chemistry reactions for creating covalent conjugates with biomolecules. In materials science, its controlled solubility facilitates fabrication of organic thin-film transistors with enhanced mobility.

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