111589
1,6-Heptadien-4-ol
97%
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About This Item
Linear Formula:
H2C=CHCH2CH(OH)CH2CH=CH2
CAS Number:
Molecular Weight:
112.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
220-742-0
MDL number:
Assay:
97%
Quality Level
assay
97%
refractive index
n20/D 1.45 (lit.)
bp
151 °C (lit.)
density
0.864 g/mL at 25 °C (lit.)
functional group
allyl, hydroxyl
SMILES string
OC(CC=C)CC=C
InChI
1S/C7H12O/c1-3-5-7(8)6-4-2/h3-4,7-8H,1-2,5-6H2
InChI key
UTGFOWQYZKTZTN-UHFFFAOYSA-N
General description
1,6-Heptadien-4-ol can help in synthesizing the derivatives of guanine, adenine, uracil and thymine via Mitsunobu condensation.
Application
1,6-Heptadien-4-ol (monoterpene alcohol) was used as the internal standard in the quantitation and identification of the important aroma components in wine. It was used to study the co- and terpolymerization reactions of carbon monoxide and propene with dicationic biphosphine palladium(II) as the catalyst.
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Validation of a Solid-Phase Microextraction Method for Headspace Analysis of Wine Aroma Components.
American Journal of Enology and Viticulture, 56(1), 37-45 (2005)
Magdalena Skotniczny et al.
Foods (Basel, Switzerland), 9(8) (2020-08-08)
The influence of fruit varieties on yeast ecology during spontaneous plum mash fermentation was investigated. Yeast colonies were isolated from mashes obtained from four plum varieties throughout fermentation in laboratory conditions during two consecutive years. The yeast strains were differentiated
Jui-Yi Tsai et al.
The Journal of organic chemistry, 68(4), 1235-1241 (2003-02-15)
A series of 1,6-heptadienes, substituted in the 4 position with nucleic acid bases 1-6, have been synthesized via Mitsunobu condensations. Guanine, adenine, thymine, and uracil derivatives can be prepared directly by coupling the protected base with 1,6-heptadien-4-ol (7). However, coupling
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 111589-5G | 04061837322754 |
| 111589-25G | 04061837322747 |