666122
α,α,α′,α′-四甲基-1,3-苯二丙酸
97%
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关于此项目
经验公式(希尔记法):
C16H22O4
化学文摘社编号:
分子量:
278.34
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
97%
表单
solid
mp
132-136 °C
官能团
carboxylic acid
SMILES字符串
CC(C)(Cc1cccc(CC(C)(C)C(O)=O)c1)C(O)=O
InChI
1S/C16H22O4/c1-15(2,13(17)18)9-11-6-5-7-12(8-11)10-16(3,4)14(19)20/h5-8H,9-10H2,1-4H3,(H,17,18)(H,19,20)
InChI key
BZWQVGTVYGEXTE-UHFFFAOYSA-N
警示用语:
Warning
危险声明
危险分类
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
Ying-Chu Chen et al.
Genes & cancer, 7(5-6), 148-153 (2016-08-24)
Protein kinases are attractive drug targets for numerous human diseases including cancers, diabetes and neurodegeneration. A number of kinase inhibitors that covalently target a cysteine residue in their target kinases have recently entered use in the cancer clinic. Despite the
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