3958-66-5 ((propan-2-yloxidanyl)

快速询单

结构式：

propan-2-yloxidanylMOL文件

CAS号：

3958-66-5

英文名称：

propan-2-yloxidanyl

分子式：

C₃H₈O

分子量：

60.09502

propan-2-yloxidanyl(3958-66-5)名称与标识符

名称

英文别名：

propan-2-yloxidanyl;Ethoxy, 1-methyl-;2-λ<sup>1</sup>-oxidanylpropane;

propan-2-yloxidanyl(3958-66-5)物化性质

实验特性

PSA : 20.23

计算特性

精确分子量 : 60.05754

propan-2-yloxidanyl(3958-66-5)相关文献

1. Visible light dye-photosensitised oxidation of pyrroles using a simple LED photoreactor
James K. Howard,Kieran J. Rihak,Christopher J. T. Hyland,Alex C. Bissember,Jason A. Smith Org. Biomol. Chem. 2016 14 8873
2. Preparation and characterization of 3,5-dinitro-1H-1,2,4-triazole
R. Haiges,G. Bélanger-Chabot,S. M. Kaplan,K. O. Christe Dalton Trans. 2015 44 7586
3. Zinc triflate catalyzed 1,3-indolylation of cyclohexanones: tandem condensation, dehydrogenation and aromatization sequence
Himanshu Singh,Rajat Tiwari,Poonam Sharma,Pramod Kumar,Nidhi Jain Org. Biomol. Chem. 2020 18 2492
4. Synthesis of 2-oxophosphorindolines via the copper-catalyzed intramolecular aromatic C–H insertion of diazophosphonamidates
Peipei Huang,Jiaxi Xu RSC Adv. 2016 6 63736
5. A direct and vicinal functionalization of the 1-methyl-2-quinolone framework: 4-alkoxylation and 3-chlorination
Feiyue Hao,Haruyasu Asahara,Nagatoshi Nishiwaki Org. Biomol. Chem. 2016 14 5128
6. Cinnolines. Part XIII. Structure and reactions of the anhydro-base of 4-hydroxy-2-methylcinnolinium hydroxide
D. E. Ames,B. Novitt J. Chem. Soc. C 1969 2355
7. Organic chemistry
J. Chem. Soc. Abstr. 1921 120 i533
8. Catalytic alcoholysis of epoxides using metal-free cucurbituril-based solids
Sofia M. Bruno,Ana C. Gomes,Tania S. M. Oliveira,Margarida M. Antunes,André D. Lopes,Anabela A. Valente,Isabel S. Gon?alves,Martyn Pillinger Org. Biomol. Chem. 2016 14 3873
9. Organic chemistry
J. Chem. Soc. Abstr. 1914 106 i1045
10. Facile P,N-heterocycle synthesis via tandem aminomethylation–cyclization of H-phosphinate building blocks
Clémence Queffélec,Jean-Luc Montchamp Org. Biomol. Chem. 2010 8 267

22739-76-0(异丙醇-d8) 21388-65-8(异丙醇-2-13C) 3979-51-9(2-丙醇-d) 19214-96-1(异丙醇-D7) 3976-29-2(异丙醇-D6氘代内标) 3972-26-7(异丙醇-D1氘代内标) 797047-27-9(N,N'-双（乙氨羰基）-S-甲基异硫脲) 79083-67-3(（1bS，4aS，7aR，7bR，8R，9R）-7b，9,9a-三羟基-3-（羟甲基）-1,1,6,8-四甲基-1,1a，1b，4,4a，7a，7b，8,9,9a-十氢-5H-环丙并[3,4]苯并[1,2-e]azulen-5-酮)

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