187523-36-0 (((3r)-3-(5-chloro-2-methoxyphenyl)-3-fluoro-6-(trifluoromethyl)-1, 3-dihydro-2h-indol-2-one)

快速询单

结构式：

(3r)-3-(5-chloro-2-methoxyphenyl)-3-fluoro-6-(trifluoromethyl)-1, 3-dihydro-2h-indol-2-oneMOL文件

CAS号：

187523-36-0

英文名称：

(3r)-3-(5-chloro-2-methoxyphenyl)-3-fluoro-6-(trifluoromethyl)-1, 3-dihydro-2h-indol-2-one

分子式：

C₁₆H₁₀ClF₄NO₂

分子量：

359.70271730423

(3r)-3-(5-chloro-2-methoxyphenyl)-3-fluoro-6-(trifluoromethyl)-1, 3-dihydro-2h-indol-2-one(187523-36-0)名称与标识符

名称

中文别名：

(3R)-3-(5-氯-2-甲氧基苯基)-3-氟-1,3-二氢-6-(三氟甲基)-2H-吲哚-2-酮;

英文别名：

(3r)-3-(5-chloro-2-methoxyphenyl)-3-fluoro-6-(trifluoromethyl)-1, 3-dihydro-2h-indol-2-one;(R)-(-)-BMS 204352;(-)-BMS-204352;(-)-MaxiPost;(R)-BMS-204352;(R)-MaxiPost;

(3r)-3-(5-chloro-2-methoxyphenyl)-3-fluoro-6-(trifluoromethyl)-1, 3-dihydro-2h-indol-2-one(187523-36-0)物化性质

实验特性

溶解度 : 几乎不溶 (0.029 g/L) (25 ºC),
密度 : 1.50±0.1 g/cm3 (20 ºC 760 Torr),

(3r)-3-(5-chloro-2-methoxyphenyl)-3-fluoro-6-(trifluoromethyl)-1, 3-dihydro-2h-indol-2-one(187523-36-0)相关文献

1. Synthetic strategies for the construction of C3-fluorinated oxindoles
Deeksha,Bittu,Ritesh Singh Org. Biomol. Chem. 2023 21 6456
2. Catalytic asymmetric fluorinations
Carla Bobbio,Véronique Gouverneur Org. Biomol. Chem. 2006 4 2065
3. Enantioselective synthesis of BMS-204352 (MaxiPost?) using N-fluoroammonium salts of cinchona alkaloids (F–CA–BF4)
Ludivine Zoute,Christophe Audouard,Jean-Christophe Plaquevent,Dominique Cahard Org. Biomol. Chem. 2003 1 1833
4. Catalytic asymmetric synthesis of hetero-substituted oxindoles
Renato Dalpozzo Org. Chem. Front. 2017 4 2063
5. Organocatalytic asymmetric syntheses of 3-fluorooxindoles containing vicinal fluoroamine motifs
Bu-Quan Zheng,Ling-Yan Chen,Jian-Bo Zhao,Jian Ji,Zi-Bin Qiu,Xinfeng Ren,Ya Li Org. Biomol. Chem. 2018 16 8989
6. Recent advances in organocatalytic methods for the synthesis of disubstituted 2- and 3-indolinones
Renato Dalpozzo,Giuseppe Bartoli,Giorgio Bencivenni Chem. Soc. Rev. 2012 41 7247
7. Chemical modulation of Kv7 potassium channels
Matteo Borgini,Pravat Mondal,Ruiting Liu,Peter Wipf RSC Med. Chem. 2021 12 483
8. Synthesis of 3-substituted 3-fluoro-2-oxindoles by deacylative alkylation
Cynthia Molina,Aitor Ortega-Martínez,José M. Sansano,Carmen Nájera Org. Biomol. Chem. 2019 17 482
9. Enantioselective halogenation reactions
Hasim Ibrahim,Antonio Togni Chem. Commun. 2004 1147
10. Solvent-specific, DAST-mediated intramolecular Friedel–Crafts reaction: access to dibenzoxepine-fused spirooxindoles
Ramesh Samikannu,Sankaranarayanan Sethuraman,Nagaraja Akula,Vignesh Radhakrishnan,Srinivasarao Kamisetti,Shabana Banu,Muthalagu Vetrichelvan,Anuradha Gupta,Jianqing Li,Richard Rampulla,Arvind Mathur Org. Biomol. Chem. 2021 19 1760

187523-36-0 (((3r)-3-(5-chloro-2-methoxyphenyl)-3-fluoro-6-(trifluoromethyl)-1, 3-dihydro-2h-indol-2-one)

(3r)-3-(5-chloro-2-methoxyphenyl)-3-fluoro-6-(trifluoromethyl)-1, 3-dihydro-2h-indol-2-one(187523-36-0)名称与标识符

名称

(3r)-3-(5-chloro-2-methoxyphenyl)-3-fluoro-6-(trifluoromethyl)-1, 3-dihydro-2h-indol-2-one(187523-36-0)物化性质

实验特性

(3r)-3-(5-chloro-2-methoxyphenyl)-3-fluoro-6-(trifluoromethyl)-1, 3-dihydro-2h-indol-2-one(187523-36-0)相关文献

目录