C9548
Coniferyl alcohol
~98% (GC)
Synonym(s):
3-(4-Hydroxy-3-methoxyphenyl)-2-propen-1-ol, 4-Hydroxy-3-methoxycinnamyl alcohol
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
HOC6H3(OCH3)CH=CHCH2OH
CAS Number:
Molecular Weight:
180.20
EC Number:
207-277-9
UNSPSC Code:
12352103
MDL number:
Beilstein/REAXYS Number:
2048961
assay
~98% (GC)
bp
163-165 °C/3 mmHg (lit.)
mp
75-80 °C (lit.)
storage temp.
−20°C
SMILES string
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+
InChI key
JMFRWRFFLBVWSI-NSCUHMNNSA-N
Looking for similar products? Visit Product Comparison Guide
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Heath D Watts et al.
Physical chemistry chemical physics : PCCP, 13(47), 20974-20985 (2011-10-20)
Five potential reaction mechanisms, each leading to the formation of an α-O-4-linked coniferyl alcohol dimer, and one scheme leading to the formation of a recently proposed free-radical coniferyl alcohol trimer were assessed using density functional theory (DFT) calculations. These potential
Chirantha P Rodrigo et al.
Journal of the American Chemical Society, 133(8), 2632-2641 (2011-02-08)
Single-conformation spectroscopy of the three lignin monomers (hereafter "monolignols") p-coumaryl alcohol (pCoumA), coniferyl alcohol (ConA), and sinapyl alcohol (SinA) has been carried out on the isolated molecules cooled in a supersonic expansion. Laser-induced fluorescence excitation, dispersed fluorescence, resonant two-photon ionization
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
Kewei Zhang et al.
The Plant cell, 24(7), 3135-3152 (2012-08-02)
Although the practice of protein engineering is industrially fruitful in creating biocatalysts and therapeutic proteins, applications of analogous techniques in the field of plant metabolic engineering are still in their infancy. Lignins are aromatic natural polymers derived from the oxidative
Yu-Chen Miao et al.
Proceedings of the National Academy of Sciences of the United States of America, 107(52), 22728-22733 (2010-12-15)
Lignin is a complex biopolymer derived primarily from the condensation of three monomeric precursors, the monolignols. The synthesis of monolignols occurs in the cytoplasm. To reach the cell wall where they are oxidized and polymerized, they must be transported across
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service