1321-16-0 ((Cyclohexene-1-carboxaldehyde)

快速询单

结构式：

Cyclohexene-1-carboxaldehydeMOL文件

CAS号：

1321-16-0

英文名称：

Cyclohexene-1-carboxaldehyde

分子式：

C₇H₁₀O

分子量：

110.153702259064

Cyclohexene-1-carboxaldehyde(1321-16-0)名称与标识符

名称

英文别名：

Cyclohexene-1-carboxaldehyde;cyclohexenecarbaldehyde;Benzaldehyde, tetrahydro-;Cyclohexenecarboxaldehyde;Tetrahydrobenzaldehyde;

标识符

InChIKey：

OANSOJSBHVENEI-UHFFFAOYSA-N

Inchi：

1S/C7H10O/c8-6-7-4-2-1-3-5-7/h4,6H,1-3,5H2

SMILES：

C1(C=O)CCCCC=1

Cyclohexene-1-carboxaldehyde(1321-16-0)物化性质

实验特性

PSA : 17.07
折射率 : 1.4670 (estimate)
沸点 : 190.95°C (rough estimate)
密度 : 0.9521 (rough estimate)

计算特性

精确分子量 : 110.0732

Cyclohexene-1-carboxaldehyde(1321-16-0)相关文献

1. Uncovering the effect of Moringa oleifera Lam. leaf addition to Fuzhuan Brick Tea on sensory properties, volatile profiles and anti-obesity activity
Xin Li,Caihong Shi,Shuxuan Wang,Shuang Wang,Xin Wang,Xin Lü Food Funct. 2023 14 2404
2. Vapochromism of indolenine-based heptamethine cyanine dye adsorbed on silica gel
Mikiko Shibayama,Yuki Uehashi,Shouhei Ajioka,Yasuhiro Kubota,Toshiyasu Inuzuka,Kazumasa Funabiki New J. Chem. 2023 47 5262
3. Synthesis, characterization and catalytic activity of novel ruthenium complexes bearing NNN click based ligands
Roberto Sole,Marco Bortoluzzi,Anke Spannenberg,Sergey Tin,Valentina Beghetto,Johannes G. de Vries Dalton Trans. 2019 48 13580
4. A three-component reaction for rapid access to underexplored 1,3-thiazine-2-thiones
Denis Kr?ger,Fabian Brockmeyer,Christoph Kahrs Org. Biomol. Chem. 2015 13 7223
5. Comprehensive two-dimensional gas chromatography with time-of-flight mass spectrometry for the screening of potent swampy/septic odor-causing compounds in two drinking water sources in China
Qingyuan Guo,Xia Li,Jianwei Yu,Haifeng Zhang,Yu Zhang,Min Yang,Ning Lu,Dong Zhang Anal. Methods 2015 7 2458
6. Environmentally benign, one-pot synthesis of pyrans by domino Knoevenagel/6π-electrocyclization in water and application to natural products
Ene Jin Jung,Byung Ho Park,Yong Rok Lee Green Chem. 2010 12 2003
7. Mechanistic understanding of molecular initiating events (MIEs) using NMR spectroscopy
Paul N. Sanderson,Wendy Simpson,Richard Cubberley,Maja Aleksic,Stephen Gutsell,Paul J. Russell Toxicol. Res. 2016 5 34
8. Effect of charge localization on the in vivo optical imaging properties of near-infrared cyanine dye/monoclonal antibody conjugates
Kazuhide Sato,Alexander P. Gorka,Tadanobu Nagaya,Megan S. Michie,Yuko Nakamura,Roger R. Nani,Vince L. Coble,Olga V. Vasalatiy,Rolf E. Swenson,Peter L. Choyke,Martin J. Schnermann,Hisataka Kobayashi Mol. BioSyst. 2016 12 3046
9. A mitochondria-targeted fluorescent dye naphthalimide-thioether-cyanine for NIR-activated photodynamic treatment of cancer cells
Ronghua Shen,Jin Bai,Ying Qian J. Mater. Chem. B 2021 9 2462
10. Molecular species fingerprinting and quantitative analysis of saffron (Crocus sativus L.) for quality control by MALDI mass spectrometry
Donatella Aiello,Carlo Siciliano,Fabio Mazzotti,Leonardo Di Donna,Constantinos M. Athanassopoulos,Anna Napoli RSC Adv. 2018 8 36104