22104-78-5 (oct-2-en-1-ol,oct-2-en-1-ol)

快速询单

结构式：

oct-2-en-1-olMOL文件

CAS号：

22104-78-5

中文名称：

oct-2-en-1-ol

英文名称：

oct-2-en-1-ol

分子式：

C₈H₁₆O

分子量：

128.21204

oct-2-en-1-ol(22104-78-5)名称与标识符

名称

英文别名：

2-Octen-1-ol;2-OCTEN-4-OL;2-Octenol;Oct-2-en-1-ol;

标识符

InChIKey：

AYQPVPFZWIQERS-VOTSOKGWSA-N

Inchi：

InChI=1S/C8H16O/c1-2-3-4-5-6-7-8-9/h6-7,9H,2-5,8H2,1H3/b7-6+

SMILES：

C(O)/C=C/CCCCC

oct-2-en-1-ol(22104-78-5)物化性质

实验特性

PSA : 20.23
折射率 : 1.4480
沸点 : 202.67°C (estimate)
熔点 : -17.5°C (estimate)
密度 : 0.8490

计算特性

精确分子量 : 128.12018

oct-2-en-1-ol(22104-78-5)相关文献

1. Correlating supercritical fluid extraction parameters with volatile compounds from Finnish wild mushrooms (Craterellus tubaeformis) and yield prediction by partial least squares regression analysis
Xiao Chen,Nghia Huynh,Heping Cui,Peng Zhou,Xiaoming Zhang,Baoru Yang RSC Adv. 2018 8 5233
2. trans-Cycloalkenes. Part I. (1RS,2RS)-trans-Cyclo-oct-2-en-1-ol
G. H. Whitham,M. Wright J. Chem. Soc. C 1971 883
3. Allylmetal-directed addition of 1O2: Scope, mechanism and synthetic utility
Patrick H. Dussault,Charles T. Eary,Richard J. Lee,Umesh R. Zope J. Chem. Soc. Perkin Trans. 1 1999 2189
4. Volatilome changes during probiotic fermentation of combined soy and rice drinks
Lorenzo Nissen,Flavia Casciano,Andrea Gianotti Food Funct. 2021 12 3159
5. Synthesis of solandelactone F, constanolactone A and an advanced intermediate towards solandelactone E from a common synthetic intermediate
Raju Yalla,Sadagopan Raghavan Org. Biomol. Chem. 2019 17 4572
6. Simultaneous inversion of configuration of both the chiral ring and the carbinol carbon in (E)-(1 R,2R)-cyclo-oct-2-en-1-ol
Ayala Balan,Herman Ziffer J. Chem. Soc. Chem. Commun. 1990 175
7. Lipid oxidation and flavor changes in saturated and unsaturated fat fractions from chicken fat during a thermal process
Dong Han,Siyang Deng,Hang Wang,Feng Huang,Marie-Laure Fauconnier,Hong Li,Jian Zheng,Linchun Meng,Chunhui Zhang,Xia Li Food Funct. 2023 14 6554
8. Control of the selectivity in multi-functional group molecules using supported gold–palladium nanoparticles
Hamed Alshammari,Peter J. Miedziak,David J. Morgan,David W. Knight,Graham J. Hutchings Green Chem. 2013 15 1244
9. trans-Cycloalkenes. Part II. Application of the dioxolan olefin synthesis to the stereospecific formation of trans-cyclo-octene derivatives. (1SR,2RS)-trans-Cyclo-oct-2-en-1-ol
G. H. Whitham,M. Wright J. Chem. Soc. C 1971 886
10. Function-oriented investigations of a peptide-based catalyst that mediates enantioselective allylic alcohol epoxidation.
Nadia C. Abascal,Phillip A. Lichtor,Michael W. Giuliano,Scott J. Miller Chem. Sci. 2014 5 4504

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