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Anthracen-2-yldiphenylphosphine oxide is a complex organic compound with the chemical formula C26H19OP. It is derived from anthracene, a polycyclic aromatic hydrocarbon, and features a phosphorus atom bonded to two phenyl groups and an oxygen atom. anthracen-2-yldiphenylphosphine oxide is known for its potential applications in the field of organic chemistry, particularly in the synthesis of various phosphorus-containing compounds. It is also used as a ligand in coordination chemistry, where it can form stable complexes with metal ions. The compound's structure and properties make it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and other specialty chemicals.

1172-98-1

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1172-98-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1172-98-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,7 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1172-98:
(6*1)+(5*1)+(4*7)+(3*2)+(2*9)+(1*8)=71
71 % 10 = 1
So 1172-98-1 is a valid CAS Registry Number.

1172-98-1Downstream Products

1172-98-1Relevant academic research and scientific papers

Palladium-Catalyzed Direct Decarbonylative Phosphorylation of Benzoic Acids with P(O)–H Compounds

Zhang, Ji-Shu,Chen, Tieqiao,Han, Li-Biao

, p. 1148 - 1153 (2020)

A direct decarbonylative phosphorylation of benzoic acids catalyzed by palladium was disclosed. Under the reaction conditions, a wide range of benzoic acids coupled readily with all the three kinds of P(O)–H compounds, i.e. secondary phosphine oxides, H-phosphinates and H-phosphonates, producing the corresponding organophosphorus compounds in good to high yields. This reaction could be conducted at a gram scale and applied in the late-stage phosphorylative modification of carboxylic acids drug molecules. These results well demonstrated the potential synthetic value of this new reaction in organic synthesis.

Aromatic phosphorus oxide compounds and preparation method for aromatic phosphorus oxide medicines of same

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Paragraph 0041-0042, (2019/12/25)

The invention discloses a plurality of aromatic phosphorus oxide compounds and a preparation method of aromatic phosphorus oxide medicines of the same. The preparation method comprises the following steps: weighing 1.2 times equivalent of aromatic carboxy

Ni-Catalyzed C-P Coupling of Aryl, Benzyl, or Allyl Ammonium Salts with P(O)H Compounds

Yang, Bo,Wang, Zhong-Xia

, p. 1500 - 1509 (2019/02/07)

A methodology that allows for the construction of C-P bonds via the nickel-catalyzed cross-coupling of organoammonium salts with appropriate phosphorus nucleophiles has been developed. Aryl-, pyridyl-, benzyl-, and allyl-ammonium triflates can be employed as the electrophiles. The employed phosphorus-based nucleophiles included diaryl/dibutyl phosphine oxide, dialkyl phosphonates, and ethyl phenylphosphinate. Functional groups OMe, CN, CF3, F, Cl, C(O)NMe2, and C(O)tBu were tolerated.

Synthesis of phosphine oxide-carboxylic acid esters bearing 9,10-dihydro-9,10-ethanoanthracene moiety

Okada, Yoshiharu,Okeya, Kazuhiro,Murata, Yoshiyasu,Aoki, Nakahisa,Aoki, Takahiro,Sugitani, Motoko,Yasui, Satomi,Sawada, Yusuke,Ogura, Fumio

, p. 821 - 829 (2007/10/03)

A bulky type of phosphine oxide-carboxylic acid bearing 9,10-dihydro-9,10-ethanoanthracene moiety was synthesized by the Diels-Alder reaction of 2-anthryldiphenylphosphine oxide and methyl acrylate, for which the structure was confirmed on the basis of s

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