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3-cyclohexene-1-carboxaldehyde oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112710-10-8

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112710-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112710-10-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,7,1 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112710-10:
(8*1)+(7*1)+(6*2)+(5*7)+(4*1)+(3*0)+(2*1)+(1*0)=68
68 % 10 = 8
So 112710-10-8 is a valid CAS Registry Number.

112710-10-8Relevant academic research and scientific papers

Acetohydroxamic acid: A new reagent for efficient synthesis of nitriles directly from aldehydes using Bi(OTf)3 as the catalyst

Sridhar, Madabhushi,Reddy, Mallu Kishore Kumar,Sairam, Vangipuram Venkata,Raveendra, Jillella,Godala, Kondal Reddy,Narsaiah, Chinthala,Ramanaiah, Beeram China,Reddy, Cirandur Suresh

, p. 3421 - 3424 (2012)

An efficient method for the preparation of nitriles directly from aldehydes by reaction with AHA using Bi(OTf)3 as the catalyst is described. Bi(OTf)3 is shown to be an efficient catalyst also for the conversion of aldoximes into nitriles.

Development of a scalable synthesis of a pyridinyl-3-azabicyclononene, a novel nicotinic partial agonist

Breining, Scott R.,Genus, John F,Mitchener, J. Pike,Cuthbertson, Timothy J,Heemstra, Ronald,Melvin, Matt S,Dull, Gary M,Yohannes, Daniel

, p. 413 - 421 (2013/06/05)

The process research and development of two syntheses of a novel nicotinic partial agonist, TC-8817 ((+)-5), are described. The original Medicinal Chemistry route had multiple flaws, making it unsuitable for further development. A second approach was expl

The 1-Aza-Cope Rearrangement

Wu, Pei-Lin,Chu, Min,Fowler, Frank W.

, p. 963 - 972 (2007/10/02)

The 1-aza-Cope rearrangement of azavinylcyclohexene derivatives were investigated.It was observed that an N-acyl substituent on the 1-aza 1,5-diene provides a sufficient driving force for this normally contrathermodynamic process.Although simple derivatives have high activation energies proceeding in relative low overall yield, a methoxy substituent at C-4 of the aza diene as well as its incorporation into strained bicyclic ring systems facilitates the 1-aza-Cope rearrangement.Because the aza diene precursors are readily available by using the Diels-Alder reaction with acrolein derivatives, this process has synthetic potential for the preparation of nitrogen heterocycles.This scheme is illustrated with the preparation of a hydrolulolidine providing a formal total synthesis of (+/-)-aspidospermine.

INTRAMOLECULAR N-ALKENYLNITRONE-ADDITIONS. REGIO- AND STEREOCHEMISTRY

Oppolzer, W.,Siles, S.,Snowden, R. L.,Bakker, B. H.,Petrzilka, M.

, p. 3497 - 3509 (2007/10/02)

Efficient intramolecular cycloadditions of N-3-alkenyl- and N-4-alkenylnitrones proceed with opposite regioselection which is modified by dipolarophile-substituent effects.Polycyclic isoxazolidines are obtained in a highly stereocontrolled fashion, consistent with an endo-addition of the Z-nitrones.

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