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5-Hexen-3-ol, 1-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-5-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

479485-75-1

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479485-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 479485-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,9,4,8 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 479485-75:
(8*4)+(7*7)+(6*9)+(5*4)+(4*8)+(3*5)+(2*7)+(1*5)=221
221 % 10 = 1
So 479485-75-1 is a valid CAS Registry Number.

479485-75-1Relevant academic research and scientific papers

Synthesis and reactivity of 1,2-dioxolanes from β,γ-epoxy ketones

Kandur, Wynne V.,Richert, Kathleen J.,Rieder, Curtis J.,Thomas, Andrew M.,Hu, Chunhua,Ziller, Joseph W.,Woerpel

supporting information, p. 2650 - 2653 (2014/06/09)

Five-membered ring peroxides were prepared in one step in 31-86% yield from readily accessible β,γ-epoxy ketones and H2O2. The reaction proceeded via a tetrahydrofuran, which was converted to the thermodynamically favored 1,2-dioxola

Stereoselective Aldol-Type Cyclization Reaction Mediated by Dibutylboron Triflate/Diisopropylethylamine

Das, Sanjib,Li, Lian-Sheng,Sinha, Subhash C.

, p. 123 - 126 (2007/10/03)

(Equation presented) Dibutylboron triflate/diisopropylethylamine mediated aldol-type cyclization provides an expedient route for the stereoselective synthesis of cyclic ethers in a single step. The method is highly efficient for the stereoselective synthe

Scandium-catalyzed allylboration of aldehydes as a practical method for highly diastereo- and enantioselective construction of homoallylic alcohols

Lachance, Hugo,Lu, Xiaosong,Gravel, Michel,Hall, Dennis G.

, p. 10160 - 10161 (2007/10/03)

A general approach for the allylation of aldehydes using stable, air-tolerant camphor-based chiral allylboronates under Sc(OTf)3 catalysis is described. This practical methodology provides both syn and anti propionate units and other homoallylic alcohols with very high levels of diastereo- and enantioselectivity for several substrates, including functionalized aliphatic aldehydes useful toward the elaboration of complex natural products. Copyright

Diastereoselective construction of cis 2,6-disubstituted tetrahydropyran rings via In(OTf)3-catalyzed intramolecular 2,5-oxonium-ene cyclization: Synthetic studies towards the total synthesis of zampanolide and dactylolide

Loh, Teck-Peng,Yang, Jian-Ying,Feng, Li-Chun,Zhou, Yan

, p. 7193 - 7196 (2007/10/03)

Diastereoselective construction of 2,6-disubstituted tetrahydropyrans with an exocyclic double bond was achieved via the In(OTf)3-catalyzed intramolecular 2,5-oxonium-ene cyclization. Its application was further demonstrated by the synthesis of

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