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)
Synthesis of (?)-homohistidine
Pirrung MC and Pei T
The Journal of Organic Chemistry, 65(7), 2229-2230 (2000)
Anne J Keurentjes et al.
Frontiers in public health, 9, 602933-602933 (2021-03-23)
Introduction: Non-melanoma skin cancer (NMSC) incidence is increasing, and occupational solar exposure contributes greatly to the overall lifetime ultraviolet radiation (UVR) dose. This is reflected in an excess risk of NMSC showing up to three-fold increase in outdoor workers. Risk
Peter D Godfrey et al.
The Journal of chemical physics, 137(6), 064306-064306 (2012-08-18)
The microwave spectra of the two conformers each, of the 1H and 3H tautomers of 4-vinylimidazole, have been measured in the 48-72 GHz spectral region. The 4-vinylimidazole was generated in situ by the facile decarboxylation of urocanic acid at its
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 859796-100G | 04061833032534 |
| 859796-5G | 04061833032541 |
| 859796-25G | 04061833552469 |