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1,2-diphenyl-1-butene-3-one oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21736-65-2

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21736-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21736-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,3 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21736-65:
(7*2)+(6*1)+(5*7)+(4*3)+(3*6)+(2*6)+(1*5)=102
102 % 10 = 2
So 21736-65-2 is a valid CAS Registry Number.

21736-65-2Downstream Products

21736-65-2Relevant academic research and scientific papers

Addition of arylboronic acids to arylpropargyl alcohols en route to indenes and quinolines

Panteleev, Jane,Huang, Richard Y.,Lui, Erica K. J.,Lautens, Mark

, p. 5314 - 5317 (2011/12/01)

A regio- and stereoselective rhodium-catalyzed synthesis of trisubstituted allylic alcohols is described. The utility of these synthons is demonstrated in a convenient synthesis of indenes and quinolines.

Isoxazole compounds as cyclooxygenase inhibitors

-

, (2008/06/13)

A class of substituted isoxazolyl compounds is described for use in treating cyclooxygenase-2 related disorders. Compounds of particular interest are defined by Formula I STR1 wherein R1, R2, and R3, are described in the specification.

SUBSTITUTED ISOXAZOLES FOR THE TREATMENT OF INFLAMMATION

-

, (2008/06/13)

A class of substituted isoxazolyl compounds is described for use in treating inflammation and inflammation-related disorders. Compounds of particular interest are defined by Formula II wherein R1 is selected from hydroxyl, lower alkyl, carboxyl, lower carboxyalkyl, lower aminocarbonylalkyl, lower alkoxycarbonylalkyl, lower aralkyl, lower alkoxyalkyl, lower aralkoxyalkyl, lower alkylthioalkyl, lower aralkylthioalkyl, lower alkylaminoalkyl, lower aryloxyalkyl, lower arylthioalkyl, lower haloalkyl, lower hydroxylalkyl, cycloalkyl, cycloalkylalkyl, and aralkyl; wherein R3 is selected from cycloalkyl, cycloalkenyl, aryl, and heteroaryl; wherein R3 is optionally substituted at a substitutable position with one or more radicals independently selected from lower alkylsulfinyl, lower alkyl, cyano, carboxyl, lower alkoxycarbonyl, lower haloalkyl, hydroxyl, lower hydroxyalkyl, lower haloalkoxy, amino, lower alkylamino, lower arylamino, lower aminoalkyl, nitro, halo, lower alkoxy, aminosulfonyl, and lower alkylthio; and wherein R4 is selected from lower alkyl, hydroxyl and amino; or a pharmaceutically-acceptable salt thereof

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