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2-(tert-butyldimethylsilanyloxymethyl)-3-phenylpropionaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

149524-96-9

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149524-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 149524-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,5,2 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 149524-96:
(8*1)+(7*4)+(6*9)+(5*5)+(4*2)+(3*4)+(2*9)+(1*6)=159
159 % 10 = 9
So 149524-96-9 is a valid CAS Registry Number.

149524-96-9Relevant academic research and scientific papers

One-pot sequential 1,4- and 1,2-reductions of α,β-unsaturated δ-lactones to the corresponding δ-lactols with CuCl and NaBH 4 in methanol

Matsumoto, Yasunobu,Yonaga, Masahiro

supporting information, p. 1764 - 1768 (2014/08/05)

An efficient, one-pot method for the highly chemoselective synthesis of δ-lactols from α,β-unsaturated δ-lactones using CuCl and NaBH4 in methanol was developed. Georg Thieme Verlag Stuttgart. New York.

Chemoenzymatic synthesis of enantiomerically enriched α-chiral 3-oxy-propionaldehydes by lipase-catalyzed kinetic resolution and desymmetrization

Wiktelius, Daniel,Larsson, Emma K.,Luthman, Kristina

, p. 2088 - 2100 (2007/10/03)

Enantiomerically enriched phenylalanine- and leucine aldehyde analogues have been prepared by lipase catalyzed desymmetrization or kinetic resolution of 1,3-propanediol derivatives as key steps. Observations of unusual enantioselectivity were made, and mo

Design and synthesis of a conformationally restricted trans peptide isostere based on the bioactive conformations of saquinavir and nelfinavir

Edmonds,Abell

, p. 3747 - 3752 (2007/10/03)

The design and synthesis of a new peptide isostere which contains a trans alkene core is described. The key step involves a Wadsworth-Emmons reaction between chiral aldehyde (2S)-9a and chiral phosphonate 7 under base-sensitive conditions to give a chiral enone (2R)-24a which was reduced to afford the desired trans alkene isosteres (2R,5R)-6a and (2R,5S)-6b (Scheme 6). A potential application of this isostere in the synthesis of HIV protease inhibitors is also discussed.

Stereoselective Epoxidation of Phe-Gly and Phe-Phe Vinyl Isosteres

Jenmalm, Annika,Berts, Wei,Li, Yi-Lin,Luthman, Kristina,Csoeregh, Ingeborg,Hacksell, Uli

, p. 1139 - 1148 (2007/10/02)

Novel Phe-Gly and Phe-Phe isosteres have been synthesized.Vinylic isosteres of Phe-Gly and Phe-Phe were prepared by facile Julia reactions, and the resulting stereoisomers were isolated and epoxidized (m-chloroperbenzoic acid).Observed stereoselectivities

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