等级
FG
Halal
Kosher
natural
质量水平
Agency
meets purity specifications of JECFA
管理合规性
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117
蒸汽密度
4.7 (vs air)
形式
liquid
折射率
n20/D 1.573 (lit.)
bp
248 °C (lit.)
mp
−1 °C (lit.)
密度
1.119 g/mL at 25 °C (lit.)
应用
flavors and fragrances
文件
see Safety & Documentation for available documents
食品过敏原
no known allergens
性状检查
anise; cherry; creamy; floral; balsamic; sweet; vanilla
SMILES字符串
[H]C(=O)c1ccc(OC)cc1
InChI
1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3
InChI key
ZRSNZINYAWTAHE-UHFFFAOYSA-N
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其他说明
天然存在：香草、茴香、八角茴香、曼越橘、黑加仑、肉桂、罗勒。
警示用语：
Warning
危险声明
危险分类
Aquatic Chronic 3 - Repr. 2
WGK
WGK 1
闪点(°F)
closed cup
闪点(°C)
closed cup
Natcha Panthama et al.
Archives of pharmacal research, 38(5), 585-590 (2014-06-11)
Two new angular types of azaphilones, isochromophilonol (1) and ochrephilonol (2), together with ten known compounds (3-12), were isolated from Chaetomium cupreum RY202. Their structures were established on the basis of spectroscopic data and the absolute configurations of 1 and
Wen-Fei He et al.
Fitoterapia, 96, 109-114 (2014-04-29)
Two new renieramycin-type bistetrahydroisoquinolinequinone alkaloids, fennebricins A (1) and B (5), and one new isoquinolinequinone alkaloid, N-formyl-1,2-dihydrorenierol (7), were isolated from the skin of the South China Sea nudibranch Jorunna funebris and its possible sponge-prey Xestospongia sp., together with eight
Navjot Kaur et al.
Antonie van Leeuwenhoek, 106(2), 301-307 (2014-05-27)
A Gram-positive, yellow pigmented strain, BKS 3-46(T) was isolated from a soil sample collected from the rhizosphere of Ficus benghalensis (banyan tree) in Bhitarkanika mangrove forest, in the Indian state of Odisha, and subjected to polyphasic taxonomic study. The 16S
Zhuozhi Wang et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 20(45), 14637-14640 (2014-10-07)
Controlled release of odorous molecules is the key to digital scent technology which will add another dimension to electronics. Photorelease is a cold mechanism that promises better temporal and spatial control than thermal release. Herein we report a novel material
Haruki Mizoguchi et al.
Organic & biomolecular chemistry, 13(21), 5955-5963 (2015-05-01)
Copper-catalyzed 6-endo cyclization of N-propargylic β-enaminocarbonyls was developed for the synthesis of oxidation-labile 1,6-dihydropyridines. This synthetic method allows flexible and regio-defined assembly of various substituents at the N1, C2, C3, C4, and C6 positions of 1,6-dihydropyridines under mild conditions.
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