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N-(3,4-dimethoxybenzyl)-N-methylnaphthalen-1-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

358335-96-3

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358335-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 358335-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,8,3,3 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 358335-96:
(8*3)+(7*5)+(6*8)+(5*3)+(4*3)+(3*5)+(2*9)+(1*6)=173
173 % 10 = 3
So 358335-96-3 is a valid CAS Registry Number.

358335-96-3Downstream Products

358335-96-3Relevant academic research and scientific papers

Expeditious approach to pyrrolophenanthridones, phenanthridines, and benzo[ c ]phenanthridines via organocatalytic direct biaryl-coupling promoted by potassium tert -butoxide

De, Subhadip,Mishra, Sourabh,Kakde, Badrinath N.,Dey, Dhananjay,Bisai, Alakesh

, p. 7823 - 7844 (2013/09/12)

A methodology involving a "transition metal-free" intramolecular biaryl-coupling of o-halo-N-arylbenzylamines has been developed in the presence of potassium tert-butoxide and an organic molecule as catalyst. The reaction appears to proceed through KOtBu-promoted intramolecular homolytic aromatic substitution (HAS). Interestingly, this biaryl coupling also works in the presence of potassium tert-butoxide as sole promoter. On extending our approach further, we found that N-acyl 2-bromo-N-arylbenzylamines undergo a one-pot N-deprotection/biaryl coupling followed by oxidation, thus offering an expeditious route to the phenanthridine and benzo[c]phenanthridine skeletons. The strategy has been applied to a concise synthesis of Amaryllidaceae alkaloids viz. oxoassoanine (1b), anhydrolycorinone (1d), 5,6-dihydrobicolorine (2d), trispheridine (2b), and benzo[c]phenanthridines alkaloids dihydronitidine (3b), dihydrochelerythidine (3d), dihydroavicine (3f), nornitidine (3h), and norchelerythrine (3j).

Novel applications of hypervalent iodine: PIFA mediated synthesis of benzo[c]phenanthiridines and benzo[c]phenanthridinones

Moreno,Tellitu,Etayo,SanMartín,Domínguez

, p. 5403 - 5411 (2007/10/03)

A short and efficient access to benzo[c]phenanthridines and phenanthridinones is achieved by the action of phenyliodine(III)-bis(trifluoroacetate) (PIFA) on properly substituted benzylnaphthylamines and naphthylbenzamides, respectively. This reagent promotes a non-phenolic oxidative biaryl coupling process, the key step of the synthesis. A study of the electronic and steric requirements of the substrates is carried out since, in some cases, dimerization processes prevail over intramolecular cyclization. A mechanistic proposal is also included.

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