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关于此项目
经验公式(希尔记法):
C10H15N3
化学文摘社编号:
分子量:
177.25
NACRES:
NA.47
PubChem Substance ID:
UNSPSC Code:
12171500
MDL number:
Quality Level
assay
97%
form
powder or crystals
technique(s)
titration: suitable
mp
80-82 °C (lit.)
application(s)
diagnostic assay manufacturing
hematology
histology
storage temp.
2-8°C
SMILES string
[N-]=[N+]=NC12C[C@H]3C[C@H](C[C@H](C3)C1)C2
InChI
1S/C10H15N3/c11-13-12-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6H2/t7-,8+,9-,10-
InChI key
JOMZSYXWYOVFEE-CHIWXEEVSA-N
Application
“反布雷特”应变分子的构建模块。
Krzysztof Matyjaszewski et al.
Molecules (Basel, Switzerland), 26(2) (2021-01-14)
N-alkyl phosphoranimines were synthesized via the Staudinger reaction of four different alkyl azides with tris(2,2,2-trifluoroethyl) phosphite. N-adamantyl, N-benzyl, N-t-butyl, and N-trityl phosphoranimines were thoroughly characterized and evaluated as chain-capping compounds in the anionic polymerization of P-tris(2,2,2-trifluoroethoxy)-N-trimethylsilyl phosphoranimine monomer. All four
Aldrichimica Acta, 18, 82-82 (1985)
Atif Sarwar et al.
PloS one, 10(4), e0123084-e0123084 (2015-05-01)
Recently, the attention of researchers has been drawn toward the synthesis of chitosan derivatives and their nanoparticles with enhanced antimicrobial activities. In this study, chitosan derivatives with different azides and alkyne groups were synthesized using click chemistry, and these were
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 276219-1G | 04061826112007 |
| 276219-5G | 04061832339184 |
