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经验公式(希尔记法):
C9H8O2
化学文摘社编号:
分子量:
148.16
FEMA编号:
2381
EC 号:
欧洲委员会编号:
535
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
13.009
NACRES:
NA.21
Agency:
meets purity specifications of JECFA
生物来源
synthetic
质量水平
等级
FG
Halal
Kosher
Agency
meets purity specifications of JECFA
管理合规性
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117
方案
≥99%
折射率
n20/D 1.556 (lit.)
沸点
272 °C (lit.)
mp
24-25 °C (lit.)
密度
1.169 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
coconut; coumarin; sweet
SMILES字符串
O=C1CCc2ccccc2O1
InChI
1S/C9H8O2/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-4H,5-6H2
InChI key
VMUXSMXIQBNMGZ-UHFFFAOYSA-N
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一般描述
二氢香豆素通常在食品和化妆品工业中用作调味成分。它天然存在于草木犀(甜三叶草)中。
应用
- 新型辐射分解诱导的二氢香豆素作为有效的酪氨酸酶抑制剂:本研究鉴定了通过辐射分解产生的新型二氢香豆素,证明了其作为有效酪氨酸酶抑制剂的潜力,这在皮肤病学及相关领域具有重要应用前景。(Jeong 等人,2024 年)(Jeong 等人,2024 年)。
生化/生理作用
10ppm 时的味道
其他说明
天然存在:草木樨和鹿舌。
警示用语:
Warning
危险声明
危险分类
Acute Tox. 4 Oral - Skin Sens. 1
储存分类代码
10 - Combustible liquids
WGK
WGK 1
闪点(°F)
>212.0 °F - closed cup
闪点(°C)
> 100 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Jie Chen et al.
The Journal of organic chemistry, 77(2), 999-1009 (2011-12-20)
A facile and enantioselective approach toward 3,4-dihydroisocoumarin was developed. The method involved an amino-thiocarbamate catalyzed enantioselective bromocyclization of styrene-type carboxylic acids, yielding 3-bromo-3,4-dihydroisocoumarins with good yields and ee's. 3-Bromo-3,4-dihydroisocoumarins are versatile building blocks for various dihydroisocoumarin derivatives in which the
Marc Vocanson et al.
Contact dermatitis, 57(6), 361-364 (2007-11-09)
There is controversy as to whether coumarin, an ingredient in cosmetics and fragrances, is a contact allergen involved in fragrance allergy. We recently showed that the purity of coumarin is a critical parameter for its allergenicity because coumarin preparations containing
S L Born et al.
Toxicology and applied pharmacology, 151(1), 45-56 (1998-08-26)
Coumarin is a known hepatotoxicant in laboratory animals, particularly rats. However, the mouse lung was identified as a major target organ in a chronic bioassay, with an oral gavage dosage of 200 mg/kg coumarin increasing the incidence of alveolar/bronchiolar adenomas
Ahmad Shaabani et al.
Organic letters, 10(12), 2581-2584 (2008-05-28)
A novel isocyanide-based four-component reaction between a 2-hydroxybenzaldehyde, Meldrum's acid, an isocyanide, and an aromatic or an aliphatic alcohol efficiently provide 3,4-dihydrocoumarin derivatives in good to excellent yields without using any catalyst or activation. The reaction can be carried out
Sharona Shachan-Tov et al.
Free radical biology & medicine, 49(10), 1516-1521 (2010-08-31)
Afri et al. reported in this journal (Free Radic. Biol. Med.32:605-618; 2002) that a direct relationship exists between the depth of alkanoylcoumarins 1 within the liposomal lipid bilayer and the rate at which they undergo superoxide-mediated saponification. These results were
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