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1H-1-Benzarsepin, 1-phenyl-, 1-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

154081-40-0

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154081-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154081-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,0,8 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 154081-40:
(8*1)+(7*5)+(6*4)+(5*0)+(4*8)+(3*1)+(2*4)+(1*0)=110
110 % 10 = 0
So 154081-40-0 is a valid CAS Registry Number.

154081-40-0Upstream product

154081-40-0Downstream Products

154081-40-0Relevant academic research and scientific papers

Studies on seven-membered heterocycles. XXXIV. Syntheses and reactions of 1-benzosilepines, 1-benzogermepines, 1-benzophosphepines, and 1-benzarsepines

Shiratori,Yasuike,Kurita,Tsuchiya

, p. 2441 - 2448 (2007/10/02)

Flash vacuum pyrolysis of 2a,7b-dihydrocyclobuta[b]-1-benzometalloles (6a-e), prepared from the corresponding 1-benzometalloles (3) containing Si, Ge, P, or As via three steps, resulted in valence isomerization with ring-opening to give 1,1-dimethyl-1-benzosilepine (7a), 1-methyl-1-phenyl-1-benzosilepine (7b), 1,1-dimethyl-1-benzogermepine (7c), 1-phenyl-1-benzophosphepine 1-oxide (7d), and 1-phenyl-1-benzarsepine 1-oxide (7e). The oxides (7d,e), on treatment with trichlorosilane, underwent deoxygenation to afford 1-phenyl-1-benzophosphepine (7f) and 1-phenyl-1-benzarsepine (7g). The 1-benzometallepines (7a-g) thus obtained are hitherto unknown heterocyclic ring compounds, and their thermal stabilities and several reactions were examined.

SYNTHESIS OF THE FIRST EXAMPLES OF 1-BENZOSILEPINE, 1-BENZOGERMEPINE, AND 1-BENZARSEPINE RING SYSTEMS

Kurita, Jyoji,Shiratori, Shinichi,Yasuike, Shuji,Tsuchiya, Takashi

, p. 2677 - 2680 (2007/10/02)

The first synthesis of 1,1-dimethyl-1-benzosilepine, 1,1-dimethyl-1-benzogermepine, and 1-phenyl-1-benzarsepines was achieved by flash vacuum pyrolysis of the dihydrocyclobutbenzoheteroles (4,7), prepared from the corresponding 1-benzoheteroles via three steps.

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