Welcome to LookChem.com Sign In|Join Free
  • or
2-Propenoic acid, 3,3-bis(4-chlorophenyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95269-22-0

Post Buying Request

95269-22-0 Suppliers

Recommended suppliers

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

95269-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95269-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,2,6 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 95269-22:
(7*9)+(6*5)+(5*2)+(4*6)+(3*9)+(2*2)+(1*2)=160
160 % 10 = 0
So 95269-22-0 is a valid CAS Registry Number.

95269-22-0Relevant academic research and scientific papers

Photoinduced Oxidative Alkoxycarbonylation of Alkenes with Alkyl Formates

Tang, Wan-Ying,Chen, Ling,Zheng, Ming,Zhan, Le-Wu,Hou, Jing,Li, Bin-Dong

supporting information, p. 3939 - 3943 (2021/05/26)

A photoinduced oxidative alkoxycarbonylation of alkenes initiated by intermolecular addition of alkoxycarbonyl radicals has been demonstrated. Employing alkyl formates as alkoxycarbonyl radical sources, a range of α,β-unsaturated esters were obtained with good regioselectivity and E selectivity under ambient conditions.

Scalable Electrochemical Dehydrogenative Lactonization of C(sp2/sp3)-H Bonds

Zhang, Sheng,Li, Lijun,Wang, Huiqiao,Li, Qian,Liu, Wenmin,Xu, Kun,Zeng, Chengchu

supporting information, p. 252 - 255 (2018/01/17)

A practical, electrochemical method is developed for the direct dehydrogenative lactonization of C(sp2/sp3)-H bonds under external oxidant- and metal-free conditions, delivering diverse lactones, including coumarin derivatives with excellent regioselectivity. The scalable nature of this newly developed electrochemical process was demonstrated on a 40 g scale following an operationally simple protocol. The remote lactonization of C(sp3)-H bonds would constitute an important synthetic advance toward electrochemical C-O bond formation.

New orally active diphenylmethyl-based ester analogues of dihydroartemisinin: Synthesis and antimalarial assessment against multidrug-resistant Plasmodium yoelii nigeriensis in mice

Chaudhary, Sandeep,Naikade, Niraj K.,Tiwari, Mohit K.,Yadav, Lalit,Shyamlal, Bharti Rajesh K.,Puri, Sunil K.

, p. 1536 - 1541 (2016/07/27)

A new series of ester analogues of artemisinin 8a–f, incorporating diphenylmethyl as pharmacologically privileged substructure, and 8g–j have been prepared and evaluated for their antimalarial activity against multidrug-resistant (MDR) Plasmodium yoelii nigeriensis in Swiss mice via oral route. These diphenylmethyl-based ester analogues 8a–f were found to be 2–4 folds more active than the antimalarial drugs β-arteether 4 and artesunic acid 5. Ester 8a, the most active compound of the series, provided complete protection to the infected mice at 24?mg/kg?×?4?days as well as 12?mg/kg?×?4?days, respectively. In this model β-arteether provided 100% and 20% protection at 48?mg/kg?×?4?days and 24?mg/kg?×?4?days, respectively.

Synthesis of coumarins via PIDA/I2-mediated oxidative cyclization of substituted phenylacrylic acids

Li, Jinming,Chen, Huiyu,Zhang-Negrerie, Daisy,Du, Yunfei,Zhao, Kang

, p. 4311 - 4320 (2013/04/24)

A variety of functionalized coumarins were synthesized from substituted phenylacrylic acids via PIDA/I2-mediated and irradiation-promoted oxidative carbon-oxygen bond formation. Our studies show that the oxygen in the pendant carboxylic acid group cyclizes favorably to the aryl ring that is cis to it. The main advantages of this method include good functional group tolerance and the transition-metal-free characteristic. The Royal Society of Chemistry 2013.

Synthesis, structure, and reactivity of dicarbene dipalladium complexes

Li, Yunfei,Yang, Longguang,Chen, Qian,Cao, Changsheng,Guan, Pei,Pang, Guangsheng,Shi, Yanhui

, p. 575 - 581 (2013/04/24)

A series of imidazole-based and benzimidazole-based di-NHC dipalladium complexes with alkyl bridges of different chain lengths were prepared. All complexes were fully characterized by NMR spectroscopy and elemental analyses. The crystal structures of three complexes were determined by X-ray diffraction. X-ray studies show the length of linker effects the solid structure of these complexes and π-π stacking plays an important role for the configuration of NHC-Pd-Py subunits. The activity of NHC-palladium complexes was investigated in the mono- and double-Heck reactions, and the imidazole-based palladium complex bearing the shortest ethylene bridge shows the best activity and selectivity in both reactions. Copyright

Controlled mono- and double-Heck reaction catalyzed by a dicarbene dipalladium complex

Li, Yunfei,Liu, Gang,Cao, Changsheng,Wang, Shuzhan,Li, Yuling,Pang, Guangsheng,Shi, Yanhui

, p. 6241 - 6250 (2013/07/27)

The phosphine-free mono- and double-Heck reaction of terminal olefins with electron-deficient and electron-rich aryl halides (iodides and bromides) is described. These reactions are catalyzed by the dicarbene dipalladium complex 1 by controlling the stoichiometry of the aryl halide and the olefine, the loading of the palladium catalyst, as well as using different base, and with or without additive. The procedure of double-Heck reaction allows β,β- diarylation and β,β′-diarylation of terminal olefins and affords trisubstituted olefins in good to excellent yields.

A novel ketone olefination via organozinc reagents in the presence of diphenyl phosphite

Cui, Hua,Li, Ying,Zhang, Songlin

supporting information, p. 2862 - 2869 (2012/11/07)

Carbonyl compounds react with organozinc reagents in the presence of diphenyl phosphite to give the corresponding olefins. A variety of 1,3-dienes and unsaturated esters were obtained in moderate to excellent yields under mild conditions. The Royal Society of Chemistry 2012.

Palladium-catalyzed double arylations of terminal olefins in acetic acid

Xu, Daichao,Lu, Chunxin,Chen, Wanzhi

experimental part, p. 1466 - 1474 (2012/03/08)

A palladium-catalyzed Heck diarylation of terminal olefins under ligand-free conditions in acetic acid is described. This procedure allows double arylation of terminal olefins affording trisubstituted olefins in good to excellent yields. The methodology is applicable to the coupling of both electron-deficient and electron-rich aryl iodides leading to symmetrical and unsymmetrical β,β-diarylated alkenes.

Palladium-catalyzed intramolecular amidation of C(sp2)-H bonds: Synthesis of 4-aryl-2-quinolinones

Inamoto, Kiyofumi,Saito, Tadataka,Hiroya, Kou,Doi, Takayuki

supporting information; experimental part, p. 3900 - 3903 (2010/07/05)

Figure presented A catalytic synthetic approach for the synthesis of 2-quinolinone compounds through a Pd-catalyzed C(sp2)-H functionalization/intramolecular amidation sequence is described. The cyclization process efficiently proceeds in the p

Novel compounds, their preparation and use

-

Page/Page column 31, (2010/02/11)

Novel compounds of the general formula (I), the use of these compounds as pharmaceutical compositions, pharmaceutical compositions comprising the compounds and methods of treatment employing these compounds and compositions. The present compounds may be u

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 95269-22-0