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2-Heptenoic acid, 5-hydroxy-7-(phenylmethoxy)-, methyl ester, (2E,5R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

869348-39-0

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869348-39-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 869348-39-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,3,4 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 869348-39:
(8*8)+(7*6)+(6*9)+(5*3)+(4*4)+(3*8)+(2*3)+(1*9)=230
230 % 10 = 0
So 869348-39-0 is a valid CAS Registry Number.

869348-39-0Relevant academic research and scientific papers

Synthesis of atorvastatin lactone linker constructs for target fishing

Sawant, Pramod,Maier, Martin E.

, p. 6576 - 6585 (2013/01/15)

With the aim of connecting atorvastatin lactone 9 to a linker for affinity-based target fishing, a concise route to the pyrrolecarboxylic acid 8 was developed. Key features of the synthesis of the diol-containing side-chain were a catalytic enantioselecti

A highly enantioselective one-pot synthesis of homoallylic alcohols via tandem asymmetric allyl transfer/olefin cross metathesis

Lee, Cheng-Hsia Angeline,Loh, Teck-Peng

, p. 809 - 812 (2007/10/03)

A highly enantioselective one-pot synthesis of linear homoallylic alcohols with terminal ester functionality has been achieved. The reactions were controlled by ordered addition of reagents and catalysts, ensuring complete consumption of aldehyde. The synthetic utility of this strategy has been demonstrated in a short synthesis of a low boiling point intermediate for grahamimycin A.

Synthesis of cis- and trans-2,5-disubstituted tetrahydrofurans by a tandem dihydroxylation-SN2 cyclization sequence

Marshall, James A.,Sabatini, Jesse J.

, p. 4819 - 4822 (2007/10/03)

(Chemical Equation Presented) Dihydroxylation of δ- and ε-mesyloxy α,β-unsaturated esters proceeds with in situ cyclization to afford 2,5-disubstituted and 2,3,5-trisubstituted tetrahydrofurans.

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