223735
松柏醇
98%
别名:
3-(4-羟基-3-甲氧基苯基)-2-丙烯-1-醇, 4-羟基-3-甲氧基肉桂醇
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关于此项目
线性分子式:
HOC6H3(OCH3)CH=CHCH2OH
化学文摘社编号:
分子量:
180.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-277-9
Beilstein/REAXYS Number:
2048961
MDL number:
Assay:
98%
Form:
solid
InChI key
JMFRWRFFLBVWSI-NSCUHMNNSA-N
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+
SMILES string
COc1cc(\C=C\CO)ccc1O
assay
98%
form
solid
bp
163-165 °C/3 mmHg (lit.)
Quality Level
solubility
alcohol: moderately soluble(lit.), diethyl ether: freely soluble(lit.), water: insoluble (almost)
functional group
hydroxyl
storage temp.
−20°C
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General description
松柏醇是eucalpytus globus酶的优先底物之一。
Application
松柏醇被用作真菌生长抑制剂。
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
Eyeshields, Gloves, type N95 (US)
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
Guilhem Reyt et al.
Nature communications, 12(1), 2320-2320 (2021-04-21)
Lignin is a complex polymer deposited in the cell wall of specialised plant cells, where it provides essential cellular functions. Plants coordinate timing, location, abundance and composition of lignin deposition in response to endogenous and exogenous cues. In roots, a
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
John H Grabber et al.
Journal of agricultural and food chemistry, 60(20), 5152-5160 (2012-04-06)
Apoplastic targeting of secondary metabolites compatible with monolignol polymerization may provide new avenues for designing lignins that are less inhibitory toward fiber fermentation. To identify suitable monolignol substitutes, primary maize cell walls were artificially lignified with normal monolignols plus various
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