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302331-54-0

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302331-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 302331-54-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,2,3,3 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 302331-54:
(8*3)+(7*0)+(6*2)+(5*3)+(4*3)+(3*1)+(2*5)+(1*4)=80
80 % 10 = 0
So 302331-54-0 is a valid CAS Registry Number.

302331-54-0Relevant articles and documents

(Z)-Ethyl 2-phenyl-1-(2-vinylphenyl)vinylcarbamates. Part 1: Synthesis and preliminary studies on their divergent transformation into benzo[c] phenanthridines and 2-phenyl-1,4-naphthoquinones

Treus, Mónica,Salas, Cristian O.,Gonazález, Marcos A.,Estévez, Juan C.,Tapia, Ricardo A.,Estévez, Ramón J.

experimental part, p. 9986 - 9995 (2011/02/23)

Treatment of N-carbethoxy-1-benzylideneisoquinolines with LDA gives N-ethoxycarbonyl-1-amino-1-(2-vinylphenyl)-2-phenylethylenes, which can easily be transformed into N-carbethoxy-1-amino-2-phenylnaphthalenes. Bischler-Napieralski reaction of these latter

A novel C-N cleavage in isoquinolines allowing the first direct transformation of 1-benzylisoquinolines into benzo[c]phenanthridines and a new route to 2-phenyl-1,4-naphthoquinones

Treus,Estevez,Castedo,Estevez

, p. 6351 - 6353 (2007/10/03)

Treatment of N-carbethoxy-1-benzylideneisoquinolines with LDA gives N-ethoxycarbonyl-1-amino-1-(2-vinylphenyl)-2-phenylethylenes, which can easily be transformed into N-carbethoxy-1-amino-2-phenyl-naphthalenes. Bichler-Napieralski reaction of these latter compounds affords the corresponding benzo[c]-phenanthridines, while their hydrolysis and subsequent oxidation constitutes a route to 2-phenyl-1,4-naphthoquinones. (C) 2000 Elsevier Science Ltd.

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