所有图片(5)
About This Item
经验公式（希尔记法）:
C10H15N3
CAS号:
分子量:
177.25
MDL號碼:
分類程式碼代碼:
12171500
PubChem物質ID:
NACRES:
NA.47
化驗
97%
形狀
powder or crystals
mp
80-82 °C (lit.)
應用
diagnostic assay manufacturing
hematology
histology
儲存溫度
2-8°C
SMILES 字串
[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 密鑰
JOMZSYXWYOVFEE-CHIWXEEVSA-N
應用
“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
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