259276
2-戊烯酸
predominantly trans, 98%
别名:
反式-2-戊烯酸
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关于此项目
线性分子式:
C2H5CH=CHCO2H
化学文摘社编号:
分子量:
100.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
237-791-9
Beilstein/REAXYS Number:
1720312
MDL number:
产品名称
2-戊烯酸, predominantly trans, 98%
InChI key
YIYBQIKDCADOSF-ONEGZZNKSA-N
InChI
1S/C5H8O2/c1-2-3-4-5(6)7/h3-4H,2H2,1H3,(H,6,7)/b4-3+
SMILES string
[H]\C(CC)=C(\[H])C(O)=O
assay
98%
form
liquid
impurities
10% cis isomer (maximum)
refractive index
n20/D 1.452 (lit.)
bp
106 °C/20 mmHg (lit.)
mp
9-11 °C (lit.)
density
0.99 g/mL at 25 °C (lit.)
functional group
carboxylic acid
Quality Level
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Application
2-Pentenoic acid has been used in preparation of new nonsteroidal human androgen receptor (hAR) agonists from an hAR antagonist pharmacophore, 2(1H)-piperidino[3,2-g]quinolinone.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
215.6 °F - closed cup
flash_point_c
102 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
L Zhi et al.
Bioorganic & medicinal chemistry letters, 9(7), 1009-1012 (1999-05-07)
New nonsteroidal human androgen receptor (hAR) agonists were developed from an hAR antagonist pharmacophore, 2(1H)-piperidino[3,2-g]quinolinone. (+/-)-trans-7,8-Diethyl-4-trifluoromethyl-2(H)-piperidino-[3,2-g]quinoli none was synthesized and demonstrated potent hAR agonist activity (EC50=3 nM) in the cell-based cotransfection assay and high binding affinity (Ki=16 nM) in the
Maximilian Benz et al.
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Inflammatory conditions are frequently accompanied by increased levels of active proteases, and there is rising interest in methods for their detection to monitor inflammation in a point of care setting. In this work, new sensor materials for disposable single-step protease
Gilles Brackman et al.
PloS one, 6(1), e16084-e16084 (2011-01-21)
Many bacteria, including Vibrio spp., regulate virulence gene expression in a cell-density dependent way through a communication process termed quorum sensing (QS). Hence, interfering with QS could be a valuable novel antipathogenic strategy. Cinnamaldehyde has previously been shown to inhibit
Joachim Morrens et al.
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