Welcome to LookChem.com Sign In|Join Free
  • or
1-(4-Fluorophenyl)ethylene-2-phosphonic acid diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81399-34-0

Post Buying Request

81399-34-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

81399-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81399-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,9 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81399-34:
(7*8)+(6*1)+(5*3)+(4*9)+(3*9)+(2*3)+(1*4)=150
150 % 10 = 0
So 81399-34-0 is a valid CAS Registry Number.

81399-34-0Relevant academic research and scientific papers

Synthesis of (E)- and (Z)-alkenylphosphonates using vinylboronates

Kabalka, George W.,Guchhait, Sankar K.

, p. 729 - 731 (2003)

(Matrix presented) (E)- and (Z)-alkenylphosphonates have been prepared stereospecifically via the reaction of vinylboronate esters with triethyl phosphite in the presence of palladium acetate.

TEMPO and Silver-Mediated Intermolecular Phosphonylation of Alkenes: Stereoselective Synthesis of (E)-Alkenylphosphonates

Wang, Lei,Yang, Zhen,Zhu, Huijuan,Liu, Haitao,Lv, Shuaipeng,Xu, Yue

supporting information, p. 2138 - 2142 (2019/03/17)

An efficient method was developed towards the synthesis of alkenylphosphonates from simple olefins and phosphonate diesters. This method was enabled by the use of cheap and commercially available silver salts and TEMPO. This method exhibits of good functional group tolerance, specific (E)-selectivity for all olefins and vinyl selectivity for aliphatic olefins. A radical mechanism was proposed, and TEMPO was involved in the product formation step.

Cu(i)/Fe(III)-Catalyzed C-P cross-coupling of styrenes with H-phosphine oxides: A facile and selective synthesis of alkenylphosphine oxides and β-ketophosphonates

Gu, Jian,Cai, Chun

supporting information, p. 4226 - 4230 (2017/07/10)

Cu(i)/Fe(iii)-Catalyzed phosphorylation and oxyphosphorylation of styrenes with H-phosphonates which can be controlled by varying the reaction temperature are developed. This study offers a new and expedient strategy for the synthesis of useful alkenylphosphine oxides and β-ketophosphonates in satisfactory yields. Moreover, the transformation is proposed to proceed via a radical process and exhibits a broad substrate scope and good functional group tolerance.

A (E) - 2-aryl ethylene cinnamenyl method for preparing ester derivative

-

Paragraph 0071-0073, (2017/03/08)

The invention discloses method for preparing (E)-2-aryl vinyl phosphonate derivatives. The method comprises the specific following steps of dissolving 1-nitro-2-aryl-vinyl derivatives, a phosphorus reagent, an accelerator manganese acetate and a catalyst copper acetate in a solvent and reacting at 20-100 DEG C to obtain the (E)-2-aryl vinyl phosphonate derivatives. According to the method disclosed by the invention, the 1-nitro-2-aryl-vinyl derivatives are adopted as starting materials, the raw materials are easily available and have multiple varieties; the products obtained by the method disclosed by the invention are multiple and can be directly applied and can be also used for other further reaction; according to the method, the use of precious metal reagents and other additives is avoided; and meanwhile, the synthetic route is short, reaction conditions are mild, the reaction operation and post-treatment process are simple, the yield is high and the method is suitable for scale production.

Manganese(iii)-mediated alkenyl Csp2-P bond formation from the reaction of β-nitrostyrenes with dialkyl phosphites

Xue, Jian-Fei,Zhou, Shao-Fang,Liu, Ye-Ye,Pan, Xiangqiang,Zou, Jian-Ping,Asekun, Olayinka Taiwo

, p. 4896 - 4902 (2015/05/05)

Mn(OAc)3-mediated tandem phosphonyl radical addition to β-nitrostyrenes followed by denitration to form (E)-2-alkenyl phosphonates in good yield is described.

A novel stereoselective synthesis of (E)-2-arylvinylphosphonates in InCl3-NaBH4-MeCN system

Wang, Chunyan,Pan, Yuanjiang,Yang, Deyu

, p. 1705 - 1709 (2007/10/03)

Hydroindation of arylalkynylphosphonates gives a intermediate which can be hydrolyzed to (E)-2-arylvinylphosphonates in InCl3-NaBH 4-MeCN system, the stereoselectivity and yield are rather high, but under the same conditions 2-alkylalkynylphosphonates do not react very well.

A novel method for the preparation of fluoroaryl- and fluoroalkyl-substituted bis- and tris-phosphonic acids

Classen,Haegele

, p. 71 - 81 (2007/10/03)

The formation of various aromatic fluorinated vinylphosphonates, geminal and vicinal bisphosphonates and trisphosphonates by the Wittig-Horner-Emmons reaction and Michael addition is presented. The regiospecific direction of Michael addition under basic c

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 81399-34-0