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1246647-95-9 (1,3-二噁烷-5-醇,化合物。与1,3-二氧戊环-4-甲醇(1:1),1,3-dioxan-5-ol:1,3-dioxolan-4-ylmethanol)

结构式：

1,3-二噁烷-5-醇,化合物。与1,3-二氧戊环-4-甲醇(1:1)结构式图片|1246647-95-9结构式图片

1,3-二噁烷-5-醇,化合物。与1,3-二氧戊环-4-甲醇(1:1)MOL文件

CAS号：

1246647-95-9

中文名称：

1,3-二噁烷-5-醇,化合物。与1,3-二氧戊环-4-甲醇(1:1)

英文名称：

1,3-dioxan-5-ol:1,3-dioxolan-4-ylmethanol

分子式：

C₈H₁₆O₆

分子量：

208.209043502808

相关分类：

溶剂及有机化学品 > 有机化合物 > Organoheterocyclic compounds > Dioxolanes > 1,3-dioxolanes

1,3-二噁烷-5-醇,化合物。与1,3-二氧戊环-4-甲醇(1:1)(1246647-95-9)名称与标识符

名称

中文别名：

1,3-二噁烷-5-醇,化合物。与1,3-二氧戊环-4-甲醇(1:1);

英文别名：

1,3-dioxan-5-ol; 1,3-dioxolan-4-ylmethanol;1,3-dioxan-5-ol;1,3-dioxolan-4-ylmethanol;(1,3-dioxolan-4-yl)methanol, 1,3-dioxan-5-ol;(1,3-dioxolan-4-yl)methanol; 1,3-dioxan-5-ol;NSC72064;3L7GR2604E;Glycerol formal, >=98.0% (GC);NSC167419;G0244;A827217;Z431564488;1,3-dioxan-5-ol:1,3-dioxolan-4-ylmethanol;1,3-Dioxan-5-ol, compd. with 1,3-dioxolane-4-methanol (1:1);

标识符

InChIKey：

JIUMSISXCKWZTA-UHFFFAOYSA-N

Inchi：

1S/2C4H8O3/c5-4-1-6-3-7-2-4;5-1-4-2-6-3-7-4/h2*4-5H,1-3H2

SMILES：

O1COCC1CO.O1COCC(C1)O

1,3-二噁烷-5-醇,化合物。与1,3-二氧戊环-4-甲醇(1:1)(1246647-95-9)物化性质

计算特性

氢键供体数量 : 2
氢键受体数量 : 6
可旋转化学键数量 : 1
重原子数量 : 14
复杂度 : 104
拓扑分子极性表面积 : 77.4

1,3-二噁烷-5-醇,化合物。与1,3-二氧戊环-4-甲醇(1:1)(1246647-95-9)相关文献

1. Upgrading of glycerol acetals by thermal catalyst-free transesterification of dialkyl carbonates under continuous-flow conditions
M. Selva,S. Guidi,M. Noè Green Chem. 2015 17 1008
2. Selective catalytic etherification of glycerol formal and solketal with dialkyl carbonates and K2CO3
Maurizio Selva,Vanni Benedet,Massimo Fabris Green Chem. 2012 14 188
3. Glycerol based solvents: synthesis, properties and applications
José I. García,Héctor García-Marín,Elísabet Pires Green Chem. 2014 16 1007
4. Glycerol acetals and ketals as bio-based solvents: positioning in Hansen and COSMO-RS spaces, volatility and stability towards hydrolysis and autoxidation
Laurianne Moity,Adrien Benazzouz,Valérie Molinier,Véronique Nardello-Rataj,Mohammed Kamal Elmkaddem,Pascale de Caro,Sophie Thiébaud-Roux,Vincent Gerbaud,Philippe Marion,Jean-Marie Aubry Green Chem. 2015 17 1779
5. Use of γ-valerolactone and glycerol derivatives as bio-based renewable solvents for membrane preparation
M. A. Rasool,I. F. J. Vankelecom Green Chem. 2019 21 1054
6. Challenges in the development of bio-based solvents: a case study on methyl(2,2-dimethyl-1,3-dioxolan-4-yl)methyl carbonate as an alternative aprotic solvent
Saimeng Jin,Fergal Byrne,Con Robert McElroy,James Sherwood,James H. Clark,Andrew J. Hunt Faraday Discuss. 2017 202 157
7. Heterogeneous acid catalysts for biodiesel production: current status and future challenges
Juan A. Melero,Jose Iglesias,Gabriel Morales Green Chem. 2009 11 1285
8. Investigation of the thermal decomposition mechanism of glycerol: the combination of a theoretical study based on the Minnesota functional and experimental support
Dongdong Zhang,Yi Cao,Pan Zhang,Jiankang Liang,Ke Xue,Yong Xia,Zhengjian Qi Phys. Chem. Chem. Phys. 2021 23 20466
9. Dimethyl carbonate: a versatile reagent for a sustainable valorization of renewables
G. Fiorani,A. Perosa,M. Selva Green Chem. 2018 20 288
10. Mesoporous Zr–SBA-16 catalysts for glycerol valorization processes: towards biorenewable formulations
Camino Gonzalez-Arellano,Leticia Parra-Rodriguez,Rafael Luque Catal. Sci. Technol. 2014 4 2287

目录

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