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Silane, (4-fluorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13272-84-9

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13272-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13272-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,7 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13272-84:
(7*1)+(6*3)+(5*2)+(4*7)+(3*2)+(2*8)+(1*4)=89
89 % 10 = 9
So 13272-84-9 is a valid CAS Registry Number.

13272-84-9Relevant academic research and scientific papers

One-pot synthesis of poly(alkoxysilane)s by Si-Si/Si-O dehydrocoupling of silanes with alcohols using Group IV and VIII metallocene complexes

Kim, Bo-Hye,Cho, Myong-Shik,Kim, Mi-Ae,Woo, Gee-Gweon

, p. 93 - 98 (2003)

Si-Si/Si-O dehydrocoupling reactions of silanes with alcohols (1:1.5 mole ratio), catalyzed by Cp2MCl2/Red-Al (M=Ti, Zr) and Cp2M′ (M′=Co, Ni), produced poly(alkoxysilane)s in one-pot in high yield. The silanes included p-X-C6H4SiH3 (X=H, CH3, OCH3, F), PhCH2SiH3, and (PhSiH2)2. The alcohols were MeOH, EtOH, iPrOH, PhOH, and CF3(CF2) 2CH2OH. The weight average molecular weight of the poly(alkoxysilane)s ranged from 600 to 8000. The dehydrocoupling reactions of phenylsilane with ethanol (1:1.5 mole ratio) using Cp2HfCl2/Red-Al and phenylsilane with ethanol (1:3 mole ratio) using Cp2TiCl2/Red-Al gave only triethoxyphenylsilane as product.

One-pot synthesis and structural characterization of poly(alkoxysilane)s catalyzed by silver-gold complexes

Cheong, Hyeonsook,Roh, Sung-Hee,Cho, Myong-Shik,Kim, Myoung-Hee,Woo, Hee-Gweon,Yang, Kap-Seung,Kim, Bo-Hye,Jun, Jin,Sohn, Honglae

, p. 702 - 705 (2013)

Combinative one-pot Si-Si/Si-O dehydrocoupling of hydrosilanes with alcohols (1:1.5 mole ratio), mediated by a mixture of AgNO3-AuCl 3 (100/1 mole ratio) rapidly produced poly(alkoxysilane)s in reasonably high yield. The addition of small amount of gold complex to the reaction mixture effectively accelerated the coupling reaction compared to the reaction rate with AgNO3 alone. The hydrosilanes include p-X-C 6H4SiH3 (X = H, CH3, OCH 3, F), PhCH2SiH3, and (PhSiH2) 2. The alcohols include MeOH, EtOH, iPrOH, PhOH, and CF 3(CF2)2CH2OH. The weight average molecular weight and polydispersity of the poly(alkoxysilane)s were in the range of 1,600~8,000 Dalton and 1.4~3.5, respectively. The dehydrocoupling reactions of phenylsilane with ethanol (1:3 mole ratio) in the presence of the Ag-Au complexes gave only triethoxyphenylsilane. Copyright

Carbon-Silicon Bond Formation in the Synthesis of Benzylic Silanes

Visco, Michael D.,Wieting, Joshua M.,Mattson, Anita E.

, p. 2883 - 2885 (2016/07/06)

Sterically encumbered organosilanes can be difficult to synthesize with conventional, strongly basic reagents; the harsh reaction conditions are often low yielding and not suitable for many functional groups. As an alternative to the typical anionic strat

Formation and characterization of silver nanoparticle composite with poly(p-Br/F-phenylsilane)

Roh, Sung-Hee,Noh, Ji Eun,Woo, Hee-Gweon,Cho, Myong-Shik,Sohn, Honglae

, p. 1760 - 1763 (2015/01/30)

The one-pot production and structural characterization of composites of silver nanoparticles with poly(p-Br/F-phenylsilane), Br/F-PPS, have been performed. The conversion of Ag+ ions to stable Ag0 nanoparticles is mediated by the cop

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