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N-(2,6-diphenyltetrahydro-2H-4-pyranyl)-acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38132-31-9

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38132-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38132-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,3 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38132-31:
(7*3)+(6*8)+(5*1)+(4*3)+(3*2)+(2*3)+(1*1)=99
99 % 10 = 9
So 38132-31-9 is a valid CAS Registry Number.

38132-31-9Downstream Products

38132-31-9Relevant academic research and scientific papers

CeCl3·7H2O/AcCl-catalyzed Prins-Ritter reaction sequence: a novel synthesis of 4-amido tetrahydropyran derivatives

Yadav,Reddy, B.V. Subba,Kumar, G.G.K.S. Narayana,Reddy, G. Madhusudhan

, p. 4903 - 4906 (2007)

Homoallylic alcohols, carbonyl compounds and nitriles undergo a smooth tandem Prins-Ritter type cyclization in the presence of CeCl3·7H2O/AcCl at ambient temperature to produce 4-amido tetrahydropyrans in high yields with all cis-sel

Molecular iodine-catalyzed, one-pot, diastereoselective synthesis of 4-amido tetrahydropyrans

Sabitha, Gowravaram,Bhikshapathi,Nayak, Sambit,Yadav

experimental part, p. 8 - 15 (2011/02/27)

A simple and efficient one-pot synthesis of symmetrical 4-amido tetrahydropyrans via the Sakurai-Prins-Ritter reaction sequence using molecular iodine as catalyst from an aldehyde and allyltrimethylsilane in acetonitrile is described. This new method has

Iodine/accl-catalyzed prins-ritter reaction: Synthesis of 4-amido tetrahydropyrans

Srinivasan,Perumal,Raja

experimental part, p. 1083 - 1091 (2011/10/01)

Homoallylic alcohols, carbonyl compounds and nitriles undergo a smooth tandem Prins-Ritter type cyclization in the presence of iodine/AcCl at room temperature to produce 4-acetamido tetrahydropyrans in high yields with all cis-selectivity.

Cerium(IV) sulfate catalyzed one-pot threecomponent diastereo selective synthesis of 4-amidotetrahydropyrans

Selvam, Nagarajan Panneer,Perumal, Paramasivan T.

supporting information; experimental part, p. 698 - 705 (2009/12/04)

A convenient and diastereoselective one-pot synthesis of cis-4-amidotetrahydropyrans is described. This simple protocol involves Prins cyclization of homoallylic alcohol and aldehydes, followed by Ritter reaction of acetonitrile leading to the formation o

A Sakurai-Prins-Ritter reaction sequence for the diastereoselective synthesis of 4-amidotetrahydropyrans catalyzed by bismuth triflate

Sabitha, Gowravaram,Bhikshapathi,Nayak, Sambit,Yadav,Ravi,Kunwar

, p. 5727 - 5731 (2008/12/22)

The synthesis of 4-amidotetrahydropyrans has been achieved by a single-step Sakurai-Prins-Ritter reaction sequence in a domino fashion by the reaction of an aldehyde and allyltrimethylsilane in acetonitrile using Bi(OTf)3 as catalyst. The prese

Stereoselective one-pot, three-component synthesis of 4- amidotetrahydropyran

Reddy,Rama Raju,Pramod Kumar,Saikia, Anil K.

, p. 1628 - 1630 (2008/09/17)

(Chemical Equation Presented) The reaction of aldehyde with allylsilane in acetonitrile mediated by boron trifluoride etherate generated 4-aminotetrahydropyrans in good yields. The product is highly stereoselective.

Three-component, one-pot diastereoselective synthesis of 4-amidotetrahydropyrans via the Prins-Ritter reaction sequence

Yadav,Reddy, B.V. Subba,Aravind,Kumar, G.G.K.S. Narayana,Madhavi,Kunwar

, p. 3025 - 3031 (2008/09/19)

Three-component coupling of carbonyl compounds, homoallylic alcohols, and nitriles has been achieved using 20 mol % of phosphomolybdic acid (PMA) at ambient temperature via the Prins-Ritter sequence to furnish 4-amidotetrahydropyrans in high yields with a

Preparation and Stereochemistry of Some Substituted 2,6-Diphenyl-4-aminotetrahydropyrans

Chandrasekrar, Nallappan,Ramalingan, Kondareddiar,Herd, Melvin D.,Berlin, K. Darrell

, p. 4352 - 4358 (2007/10/02)

Four epimeric pairs of 2,6-diphenyl-4-aminooxanes (tetrahydropyrans) have been prepared by the reduction of oximes of 2,6-diphenyl-4-oxanones. Lithium aluminum hydride reduction of oximes affords a mixture of epimeric amines rich in the equatorially subst

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