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1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-(-1-propen-1-yl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1350432-82-4

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1350432-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1350432-82-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,0,4,3 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1350432-82:
(9*1)+(8*3)+(7*5)+(6*0)+(5*4)+(4*3)+(3*2)+(2*8)+(1*2)=124
124 % 10 = 4
So 1350432-82-4 is a valid CAS Registry Number.

1350432-82-4Downstream Products

1350432-82-4Relevant academic research and scientific papers

Photoacid-Enabled Synthesis of Indanes via Formal [3 + 2] Cycloaddition of Benzyl Alcohols with Olefins

Yang, Biao,Dong, Kui,Li, Xiang-Sheng,Wu, Li-Zhu,Liu, Qiang

supporting information, p. 2040 - 2044 (2022/03/17)

An environmentally friendly and highly diastereoselective method for synthesizing indanes has been developed via a metastable-state photoacid system containing catalytic protonated merocyanine (MEH). Under visible-light irradiation, MEH yields a metastable spiro structure and liberated protons, which facilitates the formation of carbocations from benzyl alcohols, thus delivering diverse molecules in the presence of various nucleophiles. Mainly, a variety of indanes could be easily obtained from benzyl alcohols and olefins, and water is the only byproduct.

Cobalt-Catalyzed Z to e Isomerization of Alkenes: An Approach to (E)-β-Substituted Styrenes

Liu, Hongmei,Xu, Man,Cai, Cheng,Chen, Jianhui,Gu, Yugui,Xia, Yuanzhi

supporting information, p. 1193 - 1198 (2020/02/04)

An efficient cobalt-catalyzed Z to E isomerization of β-substituted styrenes using the amido-diphosphine ligand was developed, delivering the (E)-isomers with good functional tolerance and high stereoselectivity. The reaction could be scaled up to gram-scale with a catalyst loading of 0.1 mol %, using a mixture of (Z)- and (E)-alkene as the starting material. Preliminary mechanistic studies indicated that cobalt(I)-hydride and a benzylic-cobalt species were probably involved in the reaction, as supported by experiments and DFT calculations.

Catalytic wittig reactions of semi- and nonstabilized ylides enabled by ylide tuning

Coyle, Emma E.,Doonan, Bryan J.,Holohan, Andrew J.,Walsh, Killian A.,Lavigne, Florie,Krenske, Elizabeth H.,O'Brien, Christopher J.

supporting information, p. 12907 - 12911 (2016/02/18)

The first examples of catalytic Wittig reactions with semistabilized and nonstabilized ylides are reported. These reactions were enabled by utilization of a masked base, sodium tert-butyl carbonate, and/or ylide tuning. The acidity of the ylide-forming proton was tuned by varying the electron density at the phosphorus center in the precatalyst, thus facilitating the use of relatively mild bases. Steric modification of the precatalyst structure resulted in significant enhancement of E selectivity up to >95:5, E/Z. Time for a tune up: Catalytic Wittig reactions with semi- and nonstabilized ylides were enabled by use of a masked base (NaOCO2tBu) and/or ylide tuning. The acidity of the ylide-forming proton was tuned by varying the electron density at the P center in the precatalyst, thus facilitating the use of relatively mild bases. Steric modification of the precatalyst structure resulted in significant enhancement of E selectivity.

Radical cation Diels-Alder cycloadditions by visible light photocatalysis

Lin, Shishi,Ischay, Michael A.,Fry, Charles G.,Yoon, Tehshik P.

, p. 19350 - 19353 (2012/01/31)

Ruthenium(II) polypyridyl complexes promote the efficient radical cation Diels-Alder cycloaddition of electron-rich dienophiles upon irradiation with visible light. These reactions enable facile [4 + 2] cycloadditions that would be electronically mismatch

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