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关于此项目
经验公式(希尔记法):
C25H21N3O3S
化学文摘社编号:
分子量:
443.52
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47
MDL number:
产品名称
四甲-5-异硫氰酸酯,
SMILES string
CN(C)c1ccc2c(-c3ccc(cc3C([O-])=O)N=C=S)c4ccc(cc4[o+]c2c1)N(C)C
InChI key
IJSMFQNTEUNRPY-UHFFFAOYSA-N
InChI
1S/C25H21N3O3S/c1-27(2)16-6-9-19-22(12-16)31-23-13-17(28(3)4)7-10-20(23)24(19)18-8-5-15(26-14-32)11-21(18)25(29)30/h5-13H,1-4H3
assay
≥97% (HPLC)
form
powder
εmax
82-98 at 540-546 nm in methanol
application(s)
diagnostic assay manufacturing
hematology
histology
shipped in
dry ice
storage temp.
−20°C
Quality Level
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)
Rosa Micol-Ponce et al.
Plant physiology, 184(4), 2022-2039 (2020-09-12)
Ribosome biogenesis is crucial for cellular metabolism and has important implications for disease and aging. Human (Homo sapiens) glioma tumor-suppressor candidate region gene2 (GLTSCR2) and yeast (Saccharomyces cerevisiae) Nucleolar protein53 (Nop53) are orthologous proteins with demonstrated roles as ribosome biogenesis
Shuang Guo et al.
Talanta, 205, 120112-120112 (2019-08-28)
Paper-based analytical devices (PADs) are widely used in point-of-care testing (POCT) as they are cost-effective, simple and straightforward. However, poor sensitivity hinders their use in detecting diseases with low abundance biomarkers. The poor detection limit of PADs is mainly attributed
Christine M'Rini et al.
The Journal of experimental medicine, 198(9), 1301-1312 (2003-11-05)
Lymphocytes home to peripheral lymph nodes (PLNs) via high endothelial venules (HEVs) in the subcortex and incrementally larger collecting venules in the medulla. HEVs express ligands for L-selectin, which mediates lymphocyte rolling. L-selectin counterreceptors in HEVs are recognized by mAb
David Duneau et al.
BMC biology, 9, 11-11 (2011-02-24)
Infection processes consist of a sequence of steps, each critical for the interaction between host and parasite. Studies of host-parasite interactions rarely take into account the fact that different steps might be influenced by different factors and might, therefore, make
W Weninger et al.
The Journal of experimental medicine, 194(7), 953-966 (2001-10-03)
It has been proposed that two different antigen-experienced T cell subsets may be distinguishable by their preferential ability to home to lymphoid organs (central memory cells) or nonlymphoid tissues (effector memory/effector cells). We have shown recently that murine antigen-primed CD8(+)
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