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About This Item
经验公式（希尔记法）:
C9H8O5
CAS号:
分子量:
196.16
Beilstein:
209546
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
推荐产品
化驗
≥98.0%
形狀
powder
mp
158-162 °C
SMILES 字串
OC(C(O)=O)c1ccc2OCOc2c1
InChI
1S/C9H8O5/c10-8(9(11)12)5-1-2-6-7(3-5)14-4-13-6/h1-3,8,10H,4H2,(H,11,12)
InChI 密鑰
CLUJFRCEPFNVHW-UHFFFAOYSA-N
應用
3,4-(Methylenedioxy)mandelic acid was used as starting reagent in the synthesis of (-)cephalotaxine, (+)harringtonine and (-)drupacine.
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Hajer Abdelkafi et al.
Natural product reports, 29(8), 845-869 (2012-06-21)
The Cephalotaxus genus belongs to the Cephalotaxaceae family of conifers. Over the past decades it has proved to be a fruitful source of interesting natural products, especially alkaloids (cephalotaxine esters) and terpenoids (abietanes, troponoids), which often display medicinal properties, especially
Anna Constance Vind et al.
Molecular cell, 78(4), 700-713 (2020-04-15)
Impairment of ribosome function activates the MAPKKK ZAK, leading to activation of mitogen-activated protein (MAP) kinases p38 and JNK and inflammatory signaling. The mechanistic basis for activation of this ribotoxic stress response (RSR) remains completely obscure. We show that the
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