47743
4-甲酰苯氧基乙酸
≥97.0% (T)
登录查看公司和协议定价
选择尺寸
关于此项目
经验公式（希尔记法）:
C9H8O4
化学文摘社编号:
分子量:
180.16
Beilstein:
779885
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
方案
≥97.0% (T)
表单
solid
mp
193-196 °C
储存温度
2-8°C
SMILES字符串
OC(=O)COc1ccc(C=O)cc1
InChI
1S/C9H8O4/c10-5-7-1-3-8(4-2-7)13-6-9(11)12/h1-5H,6H2,(H,11,12)
InChI key
OYNIIKHNXNPSAG-UHFFFAOYSA-N
一般描述
4-Formylphenoxyacetic acid is a formylphenoxyaliphatic acid that reacts with dimedone to form 1,8-dioxo-octahydroxanthenes. It participates in the synthesis of 4-substituted benzaldehyde derivatives and 4-carboxypheoxyacetic acid.
警示用语：
Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Synthesis of 2-, 3-and 4-Carboxyphenoxyacetic Acid: A Necessary Modi?cation.
Adak MM.
Asian Journal of Chemistry, 5(2), 464-466 (1993)
Self-catalyzed syntheses, structural characterization, DPPH radical scavenging-, cytotoxicity-, and DFT studies of phenoxyaliphatic acids of 1, 8-dioxo-octahydroxanthene derivatives.
Kumar GSS, et al.
Journal of Molecular Structure, 1059, 51-60 (2014)
Wei Yi et al.
European journal of medicinal chemistry, 45(2), 639-646 (2009-11-26)
A series of novel 4-hydroxybenzaldehyde derivatives were synthesized and their inhibitory effects on the diphenolase activity of mushroom tyrosinase were investigated. Most of target compounds had more potent inhibitory activities than the parent compound 4-hydroxybenzaldehyde (IC(50)=1.22 mM). Interestingly, compound 3c
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