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2-butyl-3-phenylisoindolin-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39127-30-5

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39127-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39127-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,2 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39127-30:
(7*3)+(6*9)+(5*1)+(4*2)+(3*7)+(2*3)+(1*0)=115
115 % 10 = 5
So 39127-30-5 is a valid CAS Registry Number.

39127-30-5Downstream Products

39127-30-5Relevant academic research and scientific papers

Palladium-Catalyzed Carbonylative Synthesis of Isoindolinones from Benzylamines with TFBen as the CO Source

Fu, Lu-Yang,Ying, Jun,Qi, Xinxin,Peng, Jin-Bao,Wu, Xiao-Feng

, p. 1421 - 1429 (2019)

A palladium-catalyzed C-H carbonylation of benzylamines for the synthesis of isoindolinone scaffolds has been developed. This protocol is conducted under gas-free conditions by using benzene-1,3,5-triyl triformate (TFBen) as a convenient CO surrogate, fur

Harnessing the reactivity of Ortho-formyl-arylketones: Base-promoted regiospecific synthesis of functionalized isoquinolines

Mishra, Pawan K.,Verma, Shalini,Kumar, Manoj,Kumar, Ankit,Verma, Akhilesh K.

supporting information, p. 8278 - 8281 (2019/07/16)

An efficient and base-mediated one-pot regiospecific synthesis of structurally diversified isoquinolines and benzo[h] isoquinolines from easily accessible ortho-formyl-arylketones and aryl/(het)arylmethanamines has been described. Challenging 3-alkynyl/alkenyl isoquinolines and bis-isoquinolines were easily attained through this developed chemistry, which can be further used for various organic transformations. Operational simplicity, high atom-economy, broad substrate scope, functional group tolerance and applicability towards large scale synthesis are the advantageous features of this developed methodology.

Iodine/water-mediated oxidation of o-alkynylaroyl compounds and application of the products of oxidation in the synthesis of nitrogen heterocycles

Sakthivel, Karuppusamy,Srinivasan, Kannupal

, p. 3386 - 3396 (2013/06/27)

A facile iodine/water-mediated oxidation of the triple bond of o-alkynylaroyl compounds to furnish tricarbonyl compounds is reported. The reaction proceeds through the formation of isochromenol intermediates by the assistance of the neighbouring aroyl gro

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