추천 제품
Grade
technical grade
Quality Level
분석
80%
양식
solid
mp
61-65 °C (lit.)
작용기
hydroxyl
저장 온도
2-8°C
SMILES string
COc1cc(\C=C\CO)cc(OC)c1O
InChI
1S/C11H14O4/c1-14-9-6-8(4-3-5-12)7-10(15-2)11(9)13/h3-4,6-7,12-13H,5H2,1-2H3/b4-3+
InChI key
LZFOPEXOUVTGJS-ONEGZZNKSA-N
일반 설명
Sinapyl alcohol, a monolignol, is a primary lignin monomer.[1] It has been evaluated for anti-inflammatory and antinociceptive activities.[2] It participates in the initial stages in the biosynthesis of lignin.[3] Coupling reactions of sinapyl alcohol and sinapyl p-hydroxybenzoate has been reported.[4] Preparation of sinapyl alcohol by selective 1,2-reduction of corresponding cinnamate esters using diisobutylaluminium hydride as reducing agent has been studied.[5]
애플리케이션
Sinapyl alcohol may be employed in the preparation of lignin, a highly stable biopolymer.[6]
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
이미 열람한 고객
![4-[2-(4-Allyl-2,6-dimethoxyphenoxy)-1-hydroxypropyl]-2-methoxyphenol ≥95% (LC/MS-ELSD)](/deepweb/assets/sigmaaldrich/product/structures/103/717/7c015be4-f4aa-4720-b290-f5eaaaae5de4/640/7c015be4-f4aa-4720-b290-f5eaaaae5de4.png)
Jun Shigeto et al.
Journal of plant research, 130(1), 203-210 (2016-11-27)
Most of the known 4-coumarate:coenzyme A ligase (4CL) isoforms lack CoA-ligation activity for sinapic acid. Therefore, there is some doubt as to whether sinapic acid contributes to sinapyl alcohol biosynthesis. In this study, we characterized the enzyme activity of a
A possible mechanism for the oxidation of sinapyl alcohol by peroxidase-dependent reactions in the apoplast: enhancement of the oxidation by hydroxycinnamic acids and components of the apoplast.
Takahama U, et al.
Plant Physiology, 37(4), 499-504 (1996)
Eng-Kiat Lim et al.
FEBS letters, 579(13), 2802-2806 (2005-05-24)
This study describes the substrate recognition profile of UGT72E1, an UDP-glucose:glycosyltransferase of Arabidopsis thaliana that is the third member of a branch of glycosyltransferases, capable of conjugating lignin monomers and related metabolites. The data show that UGT72E1, in contrast to
Toshiyuki Tanaka et al.
Plant physiology, 178(2), 552-564 (2018-08-22)
Green leaf volatiles (GLVs), including six-carbon (C6) aldehydes, alcohols, and esters, are formed when plant tissues are damaged. GLVs play roles in direct plant defense at wound sites, indirect plant defense via the attraction of herbivore predators, and plant-plant communication.
Fachuang Lu et al.
Organic & biomolecular chemistry, 2(20), 2888-2890 (2004-10-14)
Cross-coupling of sinapyl p-hydroxybenzoate and sinapyl alcohol produces an 8-8-cross-coupled product that is also detected in lignifying poplar tissues, implicating sinapyl p-hydroxybenzoate as a lignin precursor.
활성 필터
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