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(Z)-4-{[tert-butyl(dimethyl)silyl]oxy}-1-cyclohexyl-3-[(trimethylsilyl)methyl]but-3-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

330444-59-2

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330444-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 330444-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,0,4,4 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 330444-59:
(8*3)+(7*3)+(6*0)+(5*4)+(4*4)+(3*4)+(2*5)+(1*9)=112
112 % 10 = 2
So 330444-59-2 is a valid CAS Registry Number.

330444-59-2Relevant academic research and scientific papers

Tandem ene-reaction/Intramolecular Sakurai Cyclisation (IMSC): A novel access to polysubstituted tetrahydropyrans and γ-butyrolactones using a unique allylation strategy

Marko, Istvan E.,Dumeunier, Raphael,Leclercq, Cedric,Leroy, Bernard,Plancher, Jean-Marc,Mekhalfia, Abdelaziz,Bayston, Daniel J.

, p. 958 - 972 (2002)

The ene-reaction between a variety of aldehydes and allylsilane 22 generates highly functionalised homoallylic alcohols 23. These adducts undergo a subsequent Intramolecular Sakurai Cyclisation (IMSC), affording in good yields polysubstituted tetrahydropyran derivatives. Furthermore, oxidative desilylation of 23 provides an efficient, connective access to a range of γ-butyrolactones and α-methylene-γ-butyrolactones.

Concise and connective synthesis of exo-methylene-γ-butyrolactones

Dumeunier, Rapha?l,Leclercq, Cédric,Markó, István E

, p. 2307 - 2311 (2007/10/03)

A novel sequence, combining an ene-reaction of the substituted allylsilane 2 with a variety of aldehydes, followed by an oxidative double desilylation, provides an efficient access to a wide range of exo-methylene-γ-butyrolactones.

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