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5-benzyl-1,3-dicyclohexylbarbituric acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16357-96-3

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16357-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16357-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,5 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16357-96:
(7*1)+(6*6)+(5*3)+(4*5)+(3*7)+(2*9)+(1*6)=123
123 % 10 = 3
So 16357-96-3 is a valid CAS Registry Number.

16357-96-3Downstream Products

16357-96-3Relevant academic research and scientific papers

Ruthenium-catalyzed selective synthesis of monoalkylated barbituric acids through “borrowing hydrogen” methodology

Putra, Anggi Eka,Oe, Yohei,Ohta, Tetsuo

, p. 1098 - 1101 (2017)

An environmentally benign alkylation of barbituric acids via “borrowing hydrogen” process with ruthenium catalysis has been established. The corresponding 5-(alkyl)barubituric acids were obtained in good to excellent yields with low catalyst loading. Vari

Iron-Catalyzed Borrowing Hydrogen C-Alkylation of Oxindoles with Alcohols

Dambatta, Mubarak B.,Polidano, Kurt,Northey, Alexander D.,Williams, Jonathan M. J.,Morrill, Louis C.

, p. 2345 - 2349 (2019/05/16)

A general and efficient iron-catalyzed C-alkylation of oxindoles has been developed. This borrowing hydrogen approach employing a (cyclopentadienone)iron carbonyl complex (2 mol %) exhibited a broad reaction scope, allowing benzylic and simple primary and secondary aliphatic alcohols to be employed as alkylating agents. A variety of oxindoles underwent selective mono-C3-alkylation in good-to-excellent isolated yields (28 examples, 50–92 % yield, 79 % average yield).

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