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Phenanthro[9,10-d][1,3]oxazole is a heterocyclic organic compound characterized by a phenanthrene core fused with a 1,3-oxazole ring. phenanthro[9,10-d][1,3]oxazole is known for its unique electronic properties and structural features, which make it a subject of interest in various fields, including organic chemistry, materials science, and medicinal chemistry. Due to its aromatic nature and potential applications in the synthesis of pharmaceuticals and other specialty chemicals, phenanthro[9,10-d][1,3]oxazole has been the focus of research for its potential use in the development of new drugs and advanced materials.

236-09-9

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236-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 236-09-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,3 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 236-09:
(5*2)+(4*3)+(3*6)+(2*0)+(1*9)=49
49 % 10 = 9
So 236-09-9 is a valid CAS Registry Number.

236-09-9Downstream Products

236-09-9Relevant academic research and scientific papers

Synthesis of Phenanthrooxazoles from 10-(Methoxyimino)phenantrene-9-one

Nicolaides, Demetrios,Varella, Evangelia,Awad, Wajih R.

, p. 7779 - 7786 (2007/10/02)

10-(Methoxyimino)phenanthren-9-one 3 easily reacts with the methyl substituted aromatics 4(a-d), as well as with α-bromo-p-xylene 6 and the α-substituted methyl derivatives 7(a-i), to afford in 5-64percent yield the corresponding 2-aryl substituted phenanthrooxazoles 5(a-g), most probably via a free radical reaction sequence.In several cases the unsubstituted oxazole 12 is also obtained, while reaction of compound 3 with the N-methyl substituted amines 7g and 14(a,b) leads to the aminooxazoles 13 and 15(a,b) respectively.

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