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11-Phenyl-10,11-dihydrodibenzo[b,f][1,4]oxazepine is a complex organic compound belonging to the class of dibenzoxazepine derivatives. It is characterized by a unique molecular structure, featuring a dibenzoxazepine core with a phenyl group at the 11th position and a dihydro functional group. 11-phenyl-10,11-dihydrodibenzo[b,f][1,4]oxazepine is primarily used in the pharmaceutical industry as an intermediate in the synthesis of various drugs, particularly those targeting the central nervous system. Its chemical properties and potential applications make it an important molecule for researchers and chemists working in the field of medicinal chemistry.

2244-56-6

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2244-56-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2244-56-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,4 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2244-56:
(6*2)+(5*2)+(4*4)+(3*4)+(2*5)+(1*6)=66
66 % 10 = 6
So 2244-56-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H15NO/c1-2-8-14(9-3-1)19-15-10-4-6-12-17(15)21-18-13-7-5-11-16(18)20-19/h1-13,19-20H

2244-56-6Downstream Products

2244-56-6Relevant academic research and scientific papers

Synthesis and enantioselective hydrogenation of seven-membered cyclic imines: Substituted dibenzo[b,f][1,4]oxazepines

Gao, Kai,Yu, Chang-Bin,Li, Wei,Zhou, Yong-Gui,Zhang, Xumu

, p. 7845 - 7847 (2011/09/13)

Highly enantioselective hydrogenation of seven-membered cyclic imines, substituted dibenzo[b,f][1,4]oxazepines, was achieved, with up to 94% ee, by using the [Ir(COD)Cl]2/(S)-Xyl-C3*-TunePhos complex as the catalyst in the presence of morpholine-HCl.

Novel domino elimination-rearrangement-addition reaction of N-alkoxy(arylmethyl)amines to N-alkyl arylamines

Miyata, Okiko,Ishikawa, Tatsuya,Ueda, Masafumi,Naito, Takeaki

, p. 2219 - 2222 (2007/10/03)

A new domino reaction of N-alkoxy(arylmethyl)amines to N-alkyl arylamines, consisting of three types of reactions: elimination of alcohol, rearrangement of the aryl group, and addition of an organolithium or a magnesium reagent, has been developed for the first time. Georg Thieme Verlag Stuttgart.

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