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N-phenyl-1,3,4-triphenyl-1,2-dihydrobenz[c-1,2]azaphosphinine 1-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1454908-98-5

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1454908-98-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1454908-98-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,4,9,0 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1454908-98:
(9*1)+(8*4)+(7*5)+(6*4)+(5*9)+(4*0)+(3*8)+(2*9)+(1*8)=195
195 % 10 = 5
So 1454908-98-5 is a valid CAS Registry Number.

1454908-98-5Downstream Products

1454908-98-5Relevant academic research and scientific papers

Microwave-Assisted Ruthenium- and Rhodium-Catalyzed Couplings of α-Amino Acid Ester-Derived Phosphinamides with Alkynes

Li, Xue-Hong,Gong, Jun-Fang,Song, Mao-Ping

, (2021/12/23)

Two different types of new phosphinamide α-amino ester derivatives have been prepared in moderate to high yields via ruthenium(II) and rhodium(III)-catalyzed ortho-C?H functionalization under microwave irradiation. Specifically, the ortho-alkenylated phosphinamides were produced through coupling of phosphinamides containing an α-substituted or α,α-disubstituted α-amino ester with internal alkynes under ruthenium catalysis. In contrast, Ru and the more effective Rh-catalyzed coupling of the α-unsubstituted glycine ester phosphinamide with alkynes resulted in formation of oxidative annulation products, phosphaisoquinolin-1-ones. The developed methods feature the use of easily accessible starting materials, short reaction time, exclusive E-stereoselectivity (for ortho-alkenylation) and good functional group tolerance. The alkenylation reaction was readily scaled up to gram scale. Furthermore, the obtained alkenylated phosphinamide could be transformed into P-containing dipeptides through hydrolysis of the ester group in the catalysis product and subsequent condensation with an α-amino ester.

NOVEL PHOSPHININE OXIDE DERIVATIVE AND PREPARATION METHOD THEREOF

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Paragraph 0426-0428; 0432-0434, (2015/12/23)

Provided are a novel phosphinine oxide derivative and a preparation method thereof, and more specifically, the phosphinine oxide derivative includes an oxaphosphinine oxide derivative and an azaphosphinine oxide derivative. The phosphinine oxide derivative according to the present invention may have a pharmacological activity and a physiological activity, and may be used as a basic framework of a natural product and may be used for development of new drug and synthesis of various medical supplies. In addition, according to the preparation method of the phosphinine oxide derivative according to the present invention, various phosphinine oxide derivatives with a high yield may be prepared by a simple synthesis process using an intramolecular annulation between a phosphinic derivative and an alkyne derivative in the presence of a rhodium (Rh) catalyst or a ruthenium (Ru) catalyst and an oxidant.

Rhodium-catalyzed oxidative coupling through C-H activation and annulation directed by phosphonamide and phosphinamide groups

Park, Sangjune,Seo, Boram,Shin, Seohyun,Son, Jeong-Yu,Lee, Phil Ho

, p. 8671 - 8673 (2013/09/23)

Rhodium-catalyzed oxidative coupling reactions via C-H activation and annulation directed by phosphonamide and phosphinamide groups were developed under aerobic conditions, which produced benzazaphosphole 1-oxides and phosphaisoquinolin-1-oxides.

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