146896-98-2 Usage
Uses
Used in Organic Synthesis:
(E)-dipropyl styrylphosphonate is used as a key intermediate for the synthesis of various organic compounds, leveraging its phosphonate nucleophilic nature to facilitate reactions and form new chemical entities.
Used in Catalyst Preparation:
DPSP serves as a valuable ligand in the preparation of catalysts, enhancing their performance and selectivity in numerous chemical processes.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (E)-dipropyl styrylphosphonate is explored for its potential to contribute to the development of new pharmaceuticals, possibly through its interaction with biopolymers and macromolecules.
Used in Materials Science:
DPSP's unique properties make it a candidate for the development of novel materials with specific characteristics, such as those required in high-tech applications or advanced manufacturing processes.
Used in Industrial Applications:
(E)-dipropyl styrylphosphonate's versatility positions it for use in various industrial applications, where its chemical reactivity and stability can be harnessed to improve or create new products and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 146896-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,8,9 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 146896-98:
(8*1)+(7*4)+(6*6)+(5*8)+(4*9)+(3*6)+(2*9)+(1*8)=192
192 % 10 = 2
So 146896-98-2 is a valid CAS Registry Number.
146896-98-2Relevant academic research and scientific papers
Silver-catalyzed synthesis of 2-arylvinylphosphonates by cross-coupling of β-nitrostyrenes with: H -phosphites
Yuan, Jin-Wei,Yang, Liang-Ru,Mao, Pu,Qu, Ling-Bo
, p. 87058 - 87065 (2016/09/23)
An efficient protocol for stereoselective synthesis of 2-arylvinylphosphonates has been developed via AgNO3-catalyzed cross-coupling of β-nitrostyrenes with dialkyl H-phosphites under mild conditions. By losing the nitro group of β-nitrostyrene
Experimental and theoretical studies on nickel-zinc-catalyzed cross-coupling of gem-dibromoalkenes with P(O)-H compounds
Liu, Liu,Lv, Ye,Wu, Yile,Gao, Xiang,Zeng, Zhiping,Gao, Yuxing,Tang, Guo,Zhao, Yufen
, p. 2322 - 2326 (2014/01/06)
A new stereoselective one-pot protocol for the preparation of E-alkenyl-phosphorus compounds under catalysis of an inexpensive nickel-zinc catalyst system has been developed, which provides a potential useful method for C-P bond formation. 31P NMR spectrum and density functional theory calculations were performed to study the reaction mechanism.
