biological source
synthetic
assay
99%
form
powder
mp
226-228 °C (lit.)
functional group
carboxylic acid
SMILES string
OC(=O)\C=C\c1c[nH]cn1
InChI
1S/C6H6N2O2/c9-6(10)2-1-5-3-7-4-8-5/h1-4H,(H,7,8)(H,9,10)/b2-1+
InChI key
LOIYMIARKYCTBW-OWOJBTEDSA-N
General description
4-咪唑丙烯酸也被称为尿烷酸,是衍生自组氨酸的一种天然代谢产物。它在300-280 nm范围内的UV-B区域具有强吸收光谱,因此可用过UV发色团。
Application
4-咪唑丙烯酸可作为前体,用于合成(±)-高组氨酸、尿酸修饰的壳聚糖、以及 N1-芳基(杂芳基)烷基-N2-[3-(1H-咪唑-4-(基)丙基]胍。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Claudia L Kleinman et al.
Nucleic acids research, 45(10), 5757-5769 (2017-03-24)
LuxR-type transcription factors control diverse physiological functions necessary for bacterial adaptation to environmental changes. In the intracellular pathogen Brucella, the LuxR homolog VjbR has been shown to regulate the expression of virulence factors acting at early stages of the intracellular
A theoretical study of the low-lying excited states of trans-and cis-urocanic acid
Page CS, et al.
The Journal of Physical Chemistry A, 103(48), 9864-9871 (1999)
Acylguanidines as bioisosteres of guanidines: N G-acylated imidazolylpropylguanidines, a new class of histamine H2 receptor agonists
Ghorai P, et al.
Journal of Medicinal Chemistry, 51(22), 7193-7204 (2008)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 859796-5G | 04061833032541 |
| 859796-25G | 04061833552469 |
| 859796-100G | 04061833032534 |