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(E)-N-(2-(1-propene-1-yl)phenyl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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72844-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72844-85-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,4 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72844-85:
(7*7)+(6*2)+(5*8)+(4*4)+(3*4)+(2*8)+(1*5)=150
150 % 10 = 0
So 72844-85-0 is a valid CAS Registry Number.

72844-85-0Relevant academic research and scientific papers

Photochemical Synthesis. Conversion of o-Vinylthioanilides to Quinolines

Mayo, Paul de,Sydnes, Leiv K.,Wenska, Grazyna

, p. 1549 - 1556 (1980)

Quinoline derivatives are formed in fair to good yields when acetonitrile solutions of o-vinylthioanilides are irradiated with Pyrex-filtered light.The transformation is a singlet reaction and involves intramolecular cycloaddition of the thioamide, yielding unstable thietanes, as the initial step.In the case of o-(1-trans-propenyl)thioacetanilide (2a) the corresponding thietane has been detected by 1H NMR spectroscopy by irradiating a toluene solution of the compound at -78 deg C.The quantum yield of quinoline formation from 2a appeared to be solvent dependent.Concomitant with quinoline formation, triplet cis-trans isomerization of the vinyl moiety takes place.In the case of 2a the quantum yield for trans -> cis isomerization is 0.506.A variable-temperature 1H NMR study of 2,3-dimethylquinoline in toluene solution has also been performed.For the 2,3-dimethylquinoline-toluene complex the enthalpy and entropy of formation are -1.03 +/- 0.10 kcal/mol and -3.7 +/- 0.2 gibbs/mol, respectively.

Copper-Catalyzed Modular Amino Oxygenation of Alkenes: Access to Diverse 1,2-Amino Oxygen-Containing Skeletons

Hemric, Brett N.,Chen, Andy W.,Wang, Qiu

supporting information, p. 1468 - 1488 (2019/01/25)

Copper-catalyzed alkene amino oxygenation reactions using O-acylhydroxylamines have been achieved for a rapid and modular access to diverse 1,2-amino oxygen-containing molecules. This transformation is applicable to the use of alcohols, carbonyls, oximes, and thio-carboxylic acids as nucleophiles on both terminal and internal alkenes. Mild reaction conditions tolerate a wide range of functional groups, including ether, ester, amide, carbamate, and halide. The reaction protocol allows for starting with free amines as the precursor of O-benzoylhydroxylamines to eliminate their isolation and purification, contributing to broader synthetic utilities. Mechanistic investigations reveal the amino oxygenation reactions may involve distinct pathways, depending on different oxygen nucleophiles.

TRIFLUOROMETHYL GROUP-CONTAINING OXAZINE AND METHOD OF PRODUCING THE SAME

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Paragraph 0050-0052, (2017/03/17)

PROBLEM TO BE SOLVED: To provide a trifluoromethyl group-containing oxazine useful as a synthetic intermediate in medical and agricultural chemical and electronic material fields, and to provide a production method suitable for industrial production. SOLU

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