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4-methyl-5-phenyl-5H-dibenzophosphole 5-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1332483-76-7

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1332483-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1332483-76-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,4,8 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1332483-76:
(9*1)+(8*3)+(7*3)+(6*2)+(5*4)+(4*8)+(3*3)+(2*7)+(1*6)=147
147 % 10 = 7
So 1332483-76-7 is a valid CAS Registry Number.

1332483-76-7Downstream Products

1332483-76-7Relevant academic research and scientific papers

Synthesis of Dibenzophospholes by Tf2O-Mediated Intramolecular Phospha-Friedel-Crafts-Type Reaction

Nishimura, Kazutoshi,Hirano, Koji,Miura, Masahiro

supporting information, p. 1467 - 1470 (2019/02/26)

A Tf2O-mediated intramolecular phospha-Friedel-Crafts-type reaction of secondary biarylphosphine oxides has been developed. The reaction is promoted simply by Tf2O to form the corresponding dibenzophospholes under metal-free conditio

Catalytic Synthesis of Chiral Phosphole Oxides via Desymmetric C-H Arylation of o -Bromoaryl Phosphine Oxides

Lin, Yan,Ma, Wei-Yang,Sun, Qiao-Ying,Cui, Yu-Ming,Xu, Li-Wen

, p. 1432 - 1436 (2017/07/22)

A palladium-catalyzed intramolecular direct arylation reaction of o -bromoaryl phosphine oxides was developed to afford a variety of P-stereogenic phosphole oxides in good yields. The enantioselectivities were closely associated with the specific structures of substrates, which ranged from 4-94%. As a result of ready availability of starting materials and simple operation to improve the enantioselectivities of the products with low ee values, the method provides a simple and straightforward procedure for the synthesis of P-stereogenic phosphole oxides.

Palladium-catalyzed direct synthesis of phosphole derivatives from triarylphosphines through cleavage of carbon-hydrogen and carbon-phosphorus bonds

Baba, Katsuaki,Tobisu, Mamoru,Chatani, Naoto

, p. 11892 - 11895 (2013/11/19)

(Phosp)hole in one: A palladium-catalyzed synthesis for directly assembling phosphole skeletons from triarylphosphines through C-H and C-P bond cleavage was developed. This approach overcomes several of the limitations of the so far reported methods. Phospholes bearing a range of functionalities (including Br, F, CO2Me, Ac, and CN) and an array of fused rings (naphthalenes, anthracenes, furans, and pyrroles) can be easily synthesized. Copyright

Palladium-catalyzed synthesis of dibenzophosphole oxides via intramolecular dehydrogenative cyclization

Kuninobu, Yoichiro,Yoshida, Takuya,Takai, Kazuhiko

, p. 7370 - 7376 (2011/11/04)

Dibenzophosphole oxides were obtained from secondary hydrophosphine oxides with a biphenyl group by dehydrogenation via phosphine-hydrogen and carbon-hydrogen bond cleavage in the presence of a catalytic amount of palladium(II) acetate, Pd(OAc)2/sub

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