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(1R,4R,5S)-4-((1S,2S)-1-hydroxy-2-methoxy-4-(4-methoxybenzyloxy)butyl)-1-((S)-4-(4-methoxybenzyloxy)-3-methylbutanoyl)-7,7-dimethyl-2-oxabicyclo[3.2.0]heptan-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

952092-51-2

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952092-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 952092-51-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,2,0,9 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 952092-51:
(8*9)+(7*5)+(6*2)+(5*0)+(4*9)+(3*2)+(2*5)+(1*1)=172
172 % 10 = 2
So 952092-51-2 is a valid CAS Registry Number.

952092-51-2Upstream product

952092-51-2Relevant academic research and scientific papers

An example of overriding cyanation during reaction of a primary alcohol with o-nitrophenyl selenocyanate

Dong, Shuzhi,Paquette, Leo A.

, p. 111 - 114 (2007)

The first example of a nitrile as the end product of a Mitsunobu substitution involving o-nitrophenyl selenocyanate and tributylphosphine is reported. Neighboring group participation operates and leads favorably to competitive formation of a 2-cyanotetrah

Pestalotiopsin A. Side chain installation and exhaustive probing of olefin metathesis as a possible tool for elaborating the cyclononene ring

Paquette, Leo A.,Dong, Shuzhi,Parker, Gregory D.

, p. 7135 - 7147 (2008/02/11)

(Chemical Equation Presented) A program directed toward an asymmetric synthesis of pestalotiopsin A is described. The routing begins with the dextrorotatory cyclobutanol 37, which is combined with the enantiomerically defined building blocks ent-15 and 16

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