B18200
氨基甲酸苄酯
99%
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线性分子式:
NH2COOCH2C6H5
化学文摘社编号:
分子量:
151.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-710-4
Beilstein/REAXYS Number:
1865635
MDL number:
产品名称
氨基甲酸苄酯, 99%
InChI key
PUJDIJCNWFYVJX-UHFFFAOYSA-N
InChI
1S/C8H9NO2/c9-8(10)11-6-7-4-2-1-3-5-7/h1-5H,6H2,(H2,9,10)
SMILES string
NC(=O)OCc1ccccc1
assay
99%
form
flakes
mp
86-89 °C (lit.)
Quality Level
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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)
Shin Ono et al.
Biopolymers, 106(4), 521-530 (2015-12-01)
Diphenyl (α-aminoalkyl)phosphonates act as mechanism-based inhibitors against serine proteases by forming a covalent bond with the hydroxy group of the active center Ser residue. Because the covalent bond was found to be broken and replaced by 2-pyridinaldoxime methiodide (2PAM), we
Sevnur Serim et al.
Organic & biomolecular chemistry, 13(8), 2293-2299 (2015-01-03)
Activity-based probes (ABPs) are powerful tools for the analysis of active enzyme species in whole proteomes, cells or animals. Quenched fluorescent ABPs (qABPs) can be applied for real time imaging, allowing the visualization of dynamic enzyme activation by fluorescent microscopy.
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