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2-phenylnaphto[1,8-de][1,3]oxazine is a complex organic chemical compound characterized by a unique molecular structure that features a naphthalene core fused with a phenyl group and an oxazine ring. 2-phenylnaphto[1,8-de][1,3]oxazine is notable for its potential applications in various fields, such as pharmaceuticals and materials science, due to its specific electronic and steric properties. The naphthalene moiety provides a stable aromatic platform, while the phenyl group offers additional π-electron delocalization, enhancing the compound's electronic characteristics. The oxazine ring introduces a nitrogen atom into the structure, which can participate in hydrogen bonding and other interactions, making 2-phenylnaphto[1,8-de][1,3]oxazine an interesting candidate for further chemical modifications and studies in the development of new drugs or functional materials.

2232-00-0

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2232-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2232-00-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,3 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2232-00:
(6*2)+(5*2)+(4*3)+(3*2)+(2*0)+(1*0)=40
40 % 10 = 0
So 2232-00-0 is a valid CAS Registry Number.

2232-00-0Downstream Products

2232-00-0Relevant academic research and scientific papers

Gas-phase thermolysis of 1-acylnaphtho[1,8-de][1,2,3]triazines. Interesting direct routes towards condensed naphtho[1,8-de]heterocyclic ring systems

Al-Awadi, Hanan,Ibrahim, Maher R.,Dib, Hicham H.,Al-Awadi, Nouria A.,Ibrahim, Yehia A.

, p. 10507 - 10513 (2007/10/03)

FVP pyrolysis of 1-acylnaphtho[1,8-de][1,2,3]triazines at 500°C and 10-2 Torr gave exclusively the corresponding 2-substituted naphtho[1,8-de][1,3]oxazines. The latter was also obtained by static pyrolysis but in lower yield along with the corresponding N-(naphthalen-1-yl)acylamides. The reaction was studied kinetically and mechanistically.

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