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α-Hexylcinnamaldehyde - 92%, high purity , CAS No.101-86-0
Basic Description
Synonyms
.alpha.-Hexylcinnamaldehyde | Epitope ID:117426 | 2-(Phenylmethylidene)octanal | 2-Hexylcinnamaldehyde | Q412025 | EC 639-566-4 | NCGC00090930-01 | .ALPHA.-HEXYLCINNAMALDEHYDE, (2E)- | EN300-18426 | NSC406799 | NSC-406799 | alpha-Hexylcinnamic aldehyde |
Specifications & Purity
≥92%
Shipped In
Normal
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Cinnamaldehydes
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Cinnamaldehydes
Alternative Parents
Benzene and substituted derivatives Enals Organic oxides Hydrocarbon derivatives Aldehydes
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Cinnamaldehyde - Benzenoid - Monocyclic benzene moiety - Enal - Alpha,beta-unsaturated aldehyde - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aldehyde - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as cinnamaldehydes. These are organic aromatic compounds containing a cinnamlaldehyde moiety, consisting of a benzene and an aldehyde group to form 3-phenylprop-2-enal.
External Descriptors
cinnamaldehydes
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
(2E)-2-benzylideneoctanal
INCHI
InChI=1S/C15H20O/c1-2-3-4-6-11-15(13-16)12-14-9-7-5-8-10-14/h5,7-10,12-13H,2-4,6,11H2,1H3/b15-12+
InChIKey
GUUHFMWKWLOQMM-NTCAYCPXSA-N
Smiles
CCCCCCC(=CC1=CC=CC=C1)C=O
Isomeric SMILES
CCCCCC/C(=C\C1=CC=CC=C1)/C=O
WGK Germany
2
RTECS
GD6560000
Molecular Weight
216.32
Beilstein
7(3)1543
Reaxy-Rn
1869613
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1869613&ln=
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Insoluble in water; Soluble in Alcohol
Sensitivity
Air Sensitive
Refractive Index
1.55
Flash Point(°F)
113 °C
Flash Point(°C)
113°C
Boil Point(°C)
175°C/15mmHg
Molecular Weight
216.320 g/mol
XLogP3
4.800
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
7
Exact Mass
216.151 Da
Monoisotopic Mass
216.151 Da
Topological Polar Surface Area
17.100 Ų
Heavy Atom Count
16
Formal Charge
0
Complexity
211.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
1
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
1
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Li Yuling, Wu Weifeng, Jian Rongchao, Ren Xiaofei, Chen Xiaole, Hong Weiqian David, Wu Min, Cai Jinglin, Lao Canyao, Xu Ximing, Sheng Zhaojun.
(2023)
Larvicidal, acetylcholinesterase inhibitory activities of four essential oils and their constituents against Aedes albopictus, and nanoemulsion preparation.
JOURNAL OF PEST SCIENCE,
96
(3):
(961-971).
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