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A31601

Sigma-Aldrich

4-Allyl-2,6-dimethoxyphenol

≥95%

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About This Item

Fórmula lineal:
H2C=CHCH2C6H2(OCH3)2OH
Número de CAS:
6627-88-9
Peso molecular:
194.23
EC Number:
229-600-2
MDL number:
MFCD00008655
UNSPSC Code:
12352100
PubChem Substance ID:
24890724
NACRES:
NA.22

assay

≥95%

form

liquid

refractive index

n20/D 1.548 (lit.)

bp

168-169 °C/11 mmHg (lit.)

density

1.092 g/mL at 25 °C (lit.)

SMILES string

COc1cc(CC=C)cc(OC)c1O

InChI

1S/C11H14O3/c1-4-5-8-6-9(13-2)11(12)10(7-8)14-3/h4,6-7,12H,1,5H2,2-3H3

InChI key

FWMPKHMKIJDEMJ-UHFFFAOYSA-N

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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2-Allylphenol 98%

Sigma-Aldrich

A34805

2-Allylphenol

Eugenol ReagentPlus®, 99%

Sigma-Aldrich

E51791

Eugenol

M Sugumaran et al.
Archives of biochemistry and biophysics, 353(2), 207-212 (1998-06-02)
Tyrosinase, which is known to possess both monophenol monooxygenase activity (EC 1.14.18.1, tyrosine, 3,4-dihydroxyphenylalanine:oxygen oxidoreductase) and o-diphenoloxidase activity (EC 1.10.3.1, o-diphenol:oxygen oxidoreductase), has been shown to exhibit other related activities. Recently, a new reaction, viz., oxidative conversion of 2,6-dimethoxyallyl phenol
Bruna Pasqualotto Costa et al.
Journal of ethnopharmacology, 267, 113645-113645 (2020-12-04)
Plant-derived compounds are a reservoir of natural chemicals and can act as drug precursors or prototypes and pharmacological probes. Methoxyeugenol is a natural compound found in plant extracts, such as nutmeg (Myristica fragrans), and it presents anthelmintic, antimicrobial, anti-inflammatory activities.
K Kónya et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 8(6), 454-459 (2002-02-05)
A series of naturally occurring 8.0.4'-neolignans (1a-d, 1g, 2g, 2h) and their analogues (le-f, lh, 1i, 2a-f, 2i) have been synthesized in racemic form starting from commercially available phenols, such as eugenol, isoeugenol and 4-allyl-2,6-dimethoxyphenol and from aromatic aldehydes, such
Supriya Agnihotri et al.
Natural product research, 26(23), 2266-2269 (2012-01-21)
Hydrodistilled oil obtained from the stem bark of Myrica esculenta Buch. Ham. ex D. Don (yield 0.3%) was analysed by capillary GC and GC-MS. The volatile oil consisted mainly of n-hexadecanol (25.2%), eudesmol acetate (21.9%), palmitic acid (11.6%), cis-β-caryophyllene (8.7%)

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