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编号:
UNSPSC代码:
12171500
PubChem化学物质编号:
NACRES:
NA.47
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方案
97%
表单
powder or crystals
技术
titration: suitable
mp
80-82 °C (lit.)
应用
diagnostic assay manufacturing
hematology
histology
储存温度
2-8°C
SMILES字符串
[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 key
JOMZSYXWYOVFEE-CHIWXEEVSA-N
应用
“反布雷特”应变分子的构建模块。
从最新的版本中选择一种：
分析证书(COA)
Lot/Batch Number
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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