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Benzenemethanol, 2-(dimethoxymethyl)-a-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

349552-84-7

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349552-84-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 349552-84-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,9,5,5 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 349552-84:
(8*3)+(7*4)+(6*9)+(5*5)+(4*5)+(3*2)+(2*8)+(1*4)=177
177 % 10 = 7
So 349552-84-7 is a valid CAS Registry Number.

349552-84-7Downstream Products

349552-84-7Relevant academic research and scientific papers

Regioselectivity in arene-catalyzed reductive lithiation of acetals of chlorobenzaldehydes

Azzena, Ugo,Dettori, Giovanna,Sforazzini, Giuseppe,Yus, Miguel,Foubelo, Francisco

, p. 1557 - 1563 (2007/10/03)

The regioselectivity of arene-catalyzed reductive lithiation of acetals of chlorobenzaldehydes strongly depends on the form of lithium metal employed as a reducing agent. According to previous findings, naphthalene catalyzed reductions run in the presence of lithium powder (high Na content) led to competitive metalations of both aromatic carbon-chlorine and benzylic carbon-oxygen bonds. At variance with these results, naphthalene catalyzed reductions run in the presence of lithium wire (either high or low Na content) led to highly regioselective metalation of aromatic carbon-chlorine bonds. These results disclose new possibilities of selective applications of arene-catalyzed reductive lithiation reactions.

Synthesis of oxa-bridged analogues of farnesyltransferase inhibitor RPR 115135

Martin,Mailliet,Maddaluno

, p. 3797 - 3805 (2007/10/03)

Two synthetic routes to new oxygen-bridged analogues of farnesyltransferase inhibitors are described that follow either a [3 + 2]/[4 + 2] or a [4 + 2]/[3 + 2] sequence of reactions. The first approach has been achieved by reacting the in situ generated phenylisobenzofuran (PIBF) 4 with pyrroline 5a and has led stereoselectively to racemic 18, which was transformed in a few steps into the target molecule 2. The second pathway relies on a key intermediate 6, obtained either by condensation of PIBF with methyl acrylate, followed by a deprotonation/selenation and an oxidation/elimination sequence, or by cycloaddition between PIBF and α-phenylselenoacrylate 11, followed by the same oxidation/elimination sequence. The reaction of 6 with amino dipole 7 gives diastereoselective access to pyrrolidine 25, a precursor of the second target 3, an epimer of 2.

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