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2H-Pyran-2-one, 5,6-dihydro-6-(2-phenylethyl)-, (6R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

350482-53-0

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350482-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 350482-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,0,4,8 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 350482-53:
(8*3)+(7*5)+(6*0)+(5*4)+(4*8)+(3*2)+(2*5)+(1*3)=130
130 % 10 = 0
So 350482-53-0 is a valid CAS Registry Number.

350482-53-0Relevant academic research and scientific papers

Iterative approach to polyketide-type structures: Stereoselective synthesis of 1,3-polyols utilizing the catalytic asymmetric Overman esterification

Binder, Joerg T.,Kirsch, Stefan F.

, p. 4164 - 4166 (2008/03/27)

An iterative systematic approach to the 1,3-polyol motif has been developed to provide access to all possible stereoisomers by utilizing the catalytic asymmetric Overman esterification for the construction of all stereogenic centres. The Royal Society of

Cytotoxic activity of (S)-goniothalamin and analogues against human cancer cells

De Fatima, Angelo,Kohn, Luciana K.,De Carvalho, Joao Ernesto,Pilli, Ronaldo A.

, p. 622 - 631 (2007/10/03)

(R)- and (S)-Goniothalamin (1) and analogues 2-9 were efficiently prepared in high overall yield and enantiomeric purity, and their cytotoxic activities were evaluated against eight human cancer cell lines. A structure-activity relationship study (SAR) al

Asymmetric allylboration for the synthesis of β-hydroxy-δ-lactone unit of statin drug analogs

Reddy, M. Venkat Ram,Brown, Herbert C.,Ramachandran, P. Veeraraghavan

, p. 239 - 243 (2007/10/03)

Acrylic esters of homoallylic alcohols prepared in 92-96% ee via the asymmetric allylboration of appropriate aldehydes with B-allyldiisopinocampheylborane, upon ring-closing metathesis in the presence of 10mol% of Grabbs' catalyst provided the correspondi

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