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Phenol, 2-[(2-naphthalenylmethylene)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78685-68-4

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78685-68-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78685-68-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,8 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78685-68:
(7*7)+(6*8)+(5*6)+(4*8)+(3*5)+(2*6)+(1*8)=194
194 % 10 = 4
So 78685-68-4 is a valid CAS Registry Number.

78685-68-4Relevant academic research and scientific papers

Base-Free and Catalyst-Free Synthesis of Functionalized Dihydrobenzoxazoles via Vinylogous Carbonate to Carbamate Rearrangement

Das, Tamal Kanti,Mondal, Santigopal,Gonnade, Rajesh G.,Biju, Akkattu T.

supporting information, p. 5597 - 5600 (2017/10/25)

An unexpected, catalyst-free, and base-free intramolecular cyclization of N-aryloxyacrylate aldimines, under thermal conditions leading to the synthesis of functionalized dihydrobenzoxazoles, is reported. The reaction features a unique rearrangement of vi

A novel dinuclear chiral niobium complex for Lewis acid catalyzed enantioselective reactions: Design of a tridentate ligand and elucidation of the catalyst structure

Kobayashi, Shu,Arai, Kenzo,Shimizu, Haruka,Ihori, Yoichi,Ishitani, Haruro,Yamashita, Yasuhiro

, p. 761 - 764 (2007/10/03)

Two's company: By using a novel chiral ligand a dinuclear chiral niobium catalyst for highly enantioselective Mannich-type reactions was developed. Tridentate binol derivatives provide excellent asymmetric environments around the niobium atom, and the Man

Photochemical and Thermal Reactions of Aromatic Schiff Bases

Tauer, Erich,Grellmann, Karl H.

, p. 4252 - 4258 (2007/10/02)

The photochemical and thermal reactions of aromatic Schiff bases (SB) prepared from o-aminophenol and aldehydes and from o-aminophenol and ketones are compared.All SB's are converted by light into the corresponding benzoxazolines.For the SB's derived from aldehydes, benzoxazoline formation is a prerequisite to convert them by a second photon into benzoxazoles.In some cases oxygen is not required for this second reaction step.SB's derived from ketones are converted into benzoxazoles by the absorption of just one photon, but only in the presence of oxygen and only if the aliphatic residue R1 of the N=C(R1R2) bridge contains at least two carbon atoms.A radical mechanism is proposed for this reaction.Benzoxazine formation is observed in some cases as a thermal side reaction.The photochemical reactions of the latter were also investigated.

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