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97960-35-5

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97960-35-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97960-35-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,9,6 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97960-35:
(7*9)+(6*7)+(5*9)+(4*6)+(3*0)+(2*3)+(1*5)=185
185 % 10 = 5
So 97960-35-5 is a valid CAS Registry Number.

97960-35-5Downstream Products

97960-35-5Relevant academic research and scientific papers

A mild and expeditious synthesis of amides from aldehydes using bio glycerol-based carbon as a recyclable catalyst

Ramesh,Narayana Murthy,Karnakar,Harsha Vardhan Reddy,Nageswar,Vijay,Prabhavathi Devi,Prasad

, p. 2636 - 2638 (2012)

The new bioglycerol-based carbon catalyst acts as an efficient, readily available, and reusable catalyst for the synthesis of amides, when aldehyde and hydroxylamine hydrochloride react in acetonitrile.

Stannous chloride dihydrate-mediated efficient access to secondary and primary amides from oximes

Ganguly, Nemai C.,Nayek, Subhasis,Chandra, Sumanta

, p. 1695 - 1702 (2014/01/17)

Highly selective, efficient and expeditious Beckmann rearrangement of a wide range of ketoximes to secondary amides (20 examples) has been accomplished using stoichiometric amount of stannous chloride dihydrate in the presence of nucleophilic additive, tetra-n-butylammonium iodide (TBAI) (10 moI%) and 4 ? MS in dry acetonitrile at reflux temperature. Aldoximes delivered primary amides through intermediacy of nitriles upon heating with an equimolar amount of SnCl2·2H2O and DBU in dry toluene at reflux in good to acceptable yields (12 examples). Utilization of mild Lewis acid, inexpensive rack reagents and procedural simplicity including easy isolation of products are key advantageous features of the protocol.

An efficient copper(II)-catalyzed direct access to primary amides from aldehydes under neat conditions

Ganguly, Nemai C.,Roy, Sushmita,Mondal, Pallab

experimental part, p. 1413 - 1416 (2012/03/27)

A simple expeditious one-pot conversion of a wide assortment of aldehydes to corresponding primary amides in good to excellent yields has been accomplished employing hydroxylamine hydrochloride (1 mol equiv), sodium acetate (1.1 mol equiv), and copper sulfate pentahydrate (5 mol %) under neat conditions at 110 °C. The protocol based upon ligand-free copper (II)-catalysis avoids the use of relatively expensive late transition metal-based catalysts, and is performed under operationally simple conditions without any demanding procedure of isolation and purification of products.

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