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(+/-)-2-[(tert-butyldimethylsilyloxy)(phenyl)methyl]-2-prop-2-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

868659-35-2

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868659-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 868659-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,6,5 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 868659-35:
(8*8)+(7*6)+(6*8)+(5*6)+(4*5)+(3*9)+(2*3)+(1*5)=242
242 % 10 = 2
So 868659-35-2 is a valid CAS Registry Number.

868659-35-2Relevant academic research and scientific papers

Diastereoselective synthesis of substituted 2-Amino-1,3-propanediols from morita Baylis-Hillman adducts

Paioti, Paulo H. S.,Rezende, Patri?cia,Coelho, Fernando

experimental part, p. 285 - 293 (2012/05/05)

We report herein a new diastereoselective approach to substituted 2-amino-1,3-propanediols with anti relative stereochemistry from Morita-Baylis-Hillman (MBH) adducts. These structural moieties have been used as intermediates for the synthesis of several

Stereoselective and diversity-oriented synthesis of trisubstituted allylic alcohols and amines

Schmidt, Yvonne,Breit, Bernhard

, p. 11789 - 11796 (2011/11/06)

Stereoselective and diversity-oriented synthesis of trisubstituted olefins was achieved by using ortho-diphenylphosphanyl benzoate (o-DPPB) as a directing group for allylic substitution. The starting point of this methodology was a set of α-methylene alde

Diastereoselective epoxidation of allylic diols derived from Baylis-Hillman adducts

Porto, Ricardo S.,Vasconcellos, Mario L. A. A.,Ventura, Elizete,Coelho, Fernando

, p. 2297 - 2306 (2007/10/03)

The results of a highly diastereoselective epoxidation of allylic diols derived from Baylis-Hillman adducts are reported. The formation of an intramolecular hydrogen bond seems to be responsible for the high anti diastereoselection obtained in this epoxid

1,4-asymmetric induction in the chromium(II)- and indium-mediated coupling of allyl bromides to aldehydes

Maguire, Robert J.,Mulzer, Johann,Bats, Jan W.

, p. 6936 - 6940 (2007/10/03)

A series of allyl bromides bearing an ethereal stereogenic substituent at C-2 were synthesized from methyl acrylate. These were coupled with a range of aldehydes under chromium(II) chloride-mediated conditions to afford syn-4-alkoxyalkan-1-ols in good yie

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