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Documenti

223735

Sigma-Aldrich

Coniferyl alcohol

98%

Sinonimo/i:

3-(4-Hydroxy-3-methoxyphenyl)-2-propen-1-ol, 4-Hydroxy-3-methoxycinnamyl alcohol

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About This Item

Formula condensata:
HOC6H3(OCH3)CH=CHCH2OH
Numero CAS:
458-35-5
Peso molecolare:
180.20
Beilstein:
2048961
Numero CE:
207-277-9
Numero MDL:
MFCD00002922
Codice UNSPSC:
12352100
ID PubChem:
24853400
NACRES:
NA.22

Saggio

98%

Forma fisica

solid

P. eboll.

163-165 °C/3 mmHg (lit.)

Punto di fusione

75-80 °C (lit.)

Solubilità

alcohol: moderately soluble(lit.)
diethyl ether: freely soluble(lit.)
water: insoluble (almost)

Temperatura di conservazione

−20°C

Stringa SMILE

COc1cc(\C=C\CO)ccc1O

InChI

1S/C10H12O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h2-5,7,11-12H,6H2,1H3/b3-2+
JMFRWRFFLBVWSI-NSCUHMNNSA-N

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Categorie correlate

Descrizione generale

Coniferyl alcohol is one of the preferred substrate of the eucalpytus globus enzyme.

Applicazioni

Coniferyl alcohol was used as a fungal growth inhibitor.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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(+)-Lariciresinol ≥95.0% (HPLC)

Sigma-Aldrich

06892

(+)-Lariciresinol

Syringaldehyde 98%

Sigma-Aldrich

S7602

Syringaldehyde

Pinoresinol analytical standard

Supelco

06709

Pinoresinol

Secoisolariciresinol ≥95.0% (HPLC)

Sigma-Aldrich

60372

Secoisolariciresinol

trans-Ferulic acid ≥99%

Sigma-Aldrich

W518301

trans-Ferulic acid

Cinnamyl alcohol 98%

Sigma-Aldrich

108197

Cinnamyl alcohol

José Renán García et al.
Plant cell reports, 33(8), 1263-1274 (2014-04-17)
The gene coding for F5H from Eucalyptus globulus was cloned and used to transform an f5h -mutant of Arabidopsis thaliana , which was complemented, thus verifying the identity of the cloned gene. Coniferaldehyde 5-hydroxylase (F5H; EC 1.14.13) is a cytochrome
Stefanie König et al.
The New phytologist, 202(3), 823-837 (2014-02-04)
Verticillium longisporum is a soil-borne vascular pathogen causing economic loss in rape. Using the model plant Arabidopsis this study analyzed metabolic changes upon fungal infection in order to identify possible defense strategies of Brassicaceae against this fungus. Metabolite fingerprinting identified
Paula Oyarce et al.
Nature plants, 5(2), 225-237 (2019-01-30)
Lignin is the main cause of lignocellulosic biomass recalcitrance to industrial enzymatic hydrolysis. By partially replacing the traditional lignin monomers by alternative ones, lignin extractability can be enhanced. To design a lignin that is easier to degrade under alkaline conditions
Alif Meem Nurani et al.
Plant & cell physiology, 61(2), 255-264 (2020-01-11)
Stem cells undergo cell division and differentiation to ensure organized tissue development. Because plant cells are immobile, plant stem cells ought to decide their cell fate prior to differentiation, to locate specialized cells in the correct position. In this study
Hsi-Chuan Chen et al.
Proceedings of the National Academy of Sciences of the United States of America, 108(52), 21253-21258 (2011-12-14)
The hydroxylation of 4- and 3-ring carbons of cinnamic acid derivatives during monolignol biosynthesis are key steps that determine the structure and properties of lignin. Individual enzymes have been thought to catalyze these reactions. In stem differentiating xylem (SDX) of
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