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3-chloro-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.

1332483-74-5

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1332483-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1332483-74-5 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 1332483-74:
(9*1)+(8*3)+(7*3)+(6*2)+(5*4)+(4*8)+(3*3)+(2*7)+(1*4)=145
145 % 10 = 5
So 1332483-74-5 is a valid CAS Registry Number.

1332483-74-5Downstream Products

1332483-74-5Relevant academic research and scientific papers

Electrosynthesis of Phosphacycles via Dehydrogenative C-P Bond Formation Using DABCO as a Mediator

Kurimoto, Yuji,Yamashita, Jun,Mitsudo, Koichi,Sato, Eisuke,Suga, Seiji

supporting information, p. 3120 - 3124 (2021/05/04)

The first electrochemical synthesis of diarylphosphole oxides (DPOs) was achieved under mild conditions. The practical protocol employs commercially available and inexpensive DABCO as a hydrogen atom transfer (HAT) mediator, leading to various DPOs in moderate to good yields. This procedure can also be applied to the synthesis of six-membered phosphacycles, such as phenophosphazine derivatives. Mechanistic studies suggested that the reaction proceeds via an electro-generated phosphinyl radical.

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

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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