登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式(希尔记法):
C14H10O3
化学文摘社编号:
分子量:
226.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-397-1
Beilstein/REAXYS Number:
1314711
MDL number:
产品名称
9-羟基-9-芴甲酸, 96%
InChI key
GXAMYUGOODKVRM-UHFFFAOYSA-N
InChI
1S/C14H10O3/c15-13(16)14(17)11-7-3-1-5-9(11)10-6-2-4-8-12(10)14/h1-8,17H,(H,15,16)
SMILES string
OC(=O)C1(O)c2ccccc2-c3ccccc13
assay
96%
mp
162-166 °C (lit.)
functional group
carboxylic acid
hydroxyl
Quality Level
正在寻找类似产品? 访问 产品对比指南
Application
9-羟基-9-芴羧酸用于合成六有机氧锡棱烷。
Vadapalli Chandrasekhar et al.
Journal of the American Chemical Society, 127(33), 11556-11557 (2005-08-18)
A hydroxyl-rich hexameric organooxotin prismane has been prepared by reaction of n-BuSn(O)OH with 9-hydroxy-9-fluorenecarboxylic acid. The supramolecular structure of this cage shows channels with hydrophobic and hydrophilic segments, which selectively entrap guest molecules.
Yusuke Nakajima et al.
Journal of experimental botany, 68(13), 3441-3456 (2017-06-22)
The direction of auxin transport changes in gravistimulated roots, causing auxin accumulation in the lower side of horizontally reoriented roots. This study found that auxin was similarly involved in hydrotropism and gravitropism in rice and pea roots, but hydrotropism in
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持