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Sigma-Aldrich

1,6-Heptadien-4-ol

97%

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About This Item

Fórmula linear:
H2C=CHCH2CH(OH)CH2CH=CH2
Número CAS:
2883-45-6
Peso molecular:
112.17
Número CE:
220-742-0
Número MDL:
MFCD00008663
Código UNSPSC:
12352100
ID de substância PubChem:
24847035
NACRES:
NA.22

Ensaio

97%

índice de refração

n20/D 1.45 (lit.)

pb

151 °C (lit.)

densidade

0.864 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

OC(CC=C)CC=C

InChI

1S/C7H12O/c1-3-5-7(8)6-4-2/h3-4,7-8H,1-2,5-6H2

chave InChI

UTGFOWQYZKTZTN-UHFFFAOYSA-N

Categorias relacionadas

Descrição geral

1,6-Heptadien-4-ol can help in synthesizing the derivatives of guanine, adenine, uracil and thymine via Mitsunobu condensation.

Aplicação

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.

Pictogramas

Flame
GHS02

Palavra indicadora

Warning

Frases de perigo

H226

Classificações de perigo

Flam. Liq. 3

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

104.0 °F - closed cup

Ponto de fulgor (°C)

40 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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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
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)
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
Tivadar Feczkó et al.
International journal of pharmaceutics, 562, 333-341 (2019-03-15)
Vinyl alcohol (VA) copolymers having fine tunable polarities are emerging materials in drug delivery applications. VA copolymers rendering well-defined molecular architecture (C/OH ratio = 2, 4, 5 and 8) were used as carriers for model drug compound, fluorescein, which exhibited significantly different
Copolymerization of carbon monoxide with exo-methylenecycloalkane and dienes: synthesis of functionalized aliphatic polyketones.
Kettunen M, et al.
Polymer International, 50(11), 1223-1227 (2001)

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