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(9S,10S)-10-Acetoxy-8,8-dimethyl-2-oxo-9,10-dihydro-2H,8H-pyrano[2,3-f]chromen-9-yl (2Z)-2-methyl-2-butenoate(CAS: 73069-27-9)
![(9S,10S)-10-Acetoxy-8,8-dimethyl-2-oxo-9,10-dihydro-2H,8H-pyrano[2,3-f]chromen-9-yl (2Z)-2-methyl-2-butenoate](https://cnstatic.chemtradehub.com/structs/730/73069-27-9-834c.webp "(9S,10S)-10-Acetoxy-8,8-dimethyl-2-oxo-9,10-dihydro-2H,8H-pyrano[2,3-f]chromen-9-yl (2Z)-2-methyl-2-butenoate")
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基本信息
分子式
C21H22O7
分子量
386.4 g/mol
物理状态
Powder
Physical Properties
沸点
486.817 ℃ at 760 mmHg
化学标识符
SMILES
CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C
InChIKey
XGPBRZDOJDLKOT-NXIDYTHLSA-N
数据库引用
MDL号
MFCD23105643
常见问题
白花前胡甲素是一种固体化合物，具有结晶形态。其分子量约为342.47 g/mol。在水中溶解度较低，但在有机溶剂如乙醇和丙酮中具有较好的溶解性。该化合物显示出一定的反应活性，特别是在酸性和碱性条件下更为敏感。
白花前胡甲素的合成通常通过多步反应完成。首先，从前胡甲素出发，通过酯化反应引入乙酰基，随后进行环化反应生成目标化合物。此过程中常用的催化剂包括硫酸和三苯基膦等，产率约为80%-90%。
白花前胡甲素在医药行业中作为天然药物的重要成分，被用于开发抗炎、抗菌和抗癌等药物。此外，它还应用于化妆品行业，作为护肤成分。
在处理白花前胡甲素时，应穿戴合适的个人防护装备（PPE），如实验服、手套和护目镜。在通风橱内操作，确保良好的通风。一旦发生泄露，应立即清理，并使用吸水纸或沙子吸收。参考安全数据表（SDS）获取详细的安全信息。
安全须知
使用前请验证产品规格和安全数据。联系供应商获取详细安全信息。
请始终遵循正确的操作程序