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(S)-2-<<(Benzyloxy)methoxy>methoxy>-3-<(tert-butyldiphenylsilyl)oxy>-1-propanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138436-40-5

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138436-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138436-40-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,3 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 138436-40:
(8*1)+(7*3)+(6*8)+(5*4)+(4*3)+(3*6)+(2*4)+(1*0)=135
135 % 10 = 5
So 138436-40-5 is a valid CAS Registry Number.

138436-40-5Relevant academic research and scientific papers

Practical enzymatic desymmetrization of 2-(ethoxycarbonyl)propane-1,3-diyl dihexanoate and model cyclization for the A-D ring system of lysergic acid

Miyata, Sachiho,Kumamoto, Takuya,Ishikawa, Tsutomu

, p. 1420 - 1438 (2008/02/08)

Porcine pancreas lipase-catalyzed hydrolysis of symmetrical 2-(ethoxycarbonyl)propane-1,3-diyl dihexanoate, under the modified conditions of the Seebach protocol, afforded a desymmetrized monohexanoate in 40-51% yield with 91-94% ee, even in a gram-scale reaction. The absolute configuration of a half-hydrolyzed (-)-product was determined to be (R) by conversion to a known 2-methylpropane-1,3-diol derivative. Samarium iodide-induced radical cyclization of 2-oxo-3-phenylethylamine with a C4 unit on the N-atom, derived from the racemic monohexanoate, afforded a 3-phenylpiperidine derivative as a model construction of the A-D ring system of lysergic acid.

Chemoenzymatic Preparation of Asymmetrized Tris(hydroxymethyl)methane (THYM*) and of Asymmetrized Bis(hydroxymethyl)acetaldehyde (BHYMA*) as New Highly Versatile Chiral Building Blocks

Guanti, Giuseppe,Banfi, Luca,Narisano, Enrica

, p. 1540 - 1554 (2007/10/02)

A series of asymmetrized tris(hydroxymethyl)methanes 2 and bis(hydroxymethyl)acetaldehydes 3 have been prepared in both enantiomeric forms through a chemoenzymatic methodology.The key step is the highly enantioselective PPL-catalyzed monohydrolysis of 2(E)-alkenyl-1,3-diacetoxypropanes 25-27.A careful study on the effect of unsaturations adjacent to the prochiral center in a series of 2-substituted 1,3-diacetoxypropanes has confirmed the suggested beneficial effect of a ? system in that position but has also unveiled an unprecedented dramatic effect of double-bond configuration on enantioselectivity.A new empirical model for the interpretation of these and other results, based both on polarity and steric arguments, is proposed.This study provides a general protocol for the efficient synthesis of asymmetrized 1,3-propanediols bearing in position 2 saturated or unsaturated carbon chains.

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