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质量水平
方案
≥96%
表单
liquid
反应适用性
reaction type: click chemistry
折射率
n20/D 1.461
密度
1.095 g/mL at 25 °C
储存温度
2-8°C
SMILES字符串
OCCCN=[N+]=[N-]
InChI
1S/C3H7N3O/c4-6-5-2-1-3-7/h7H,1-3H2
InChI key
WHVSIWLMCCGHFW-UHFFFAOYSA-N
一般描述
3-叠氮基-1-丙醇是一种含叠氮试剂,用于应变促进的叠氮化物-炔烃环加成反应(SPAAC)。 这让我们实现生物分子的选择性和无铜电极化学修饰。
应用
3-叠氮基-1-丙醇可用作:
- 合成杂环化合物(如二氢噁嗪)的前体
- 通过1,3-偶极环加成反应合成杂官能团聚酯的试剂
历史批次信息供参考:
分析证书(COA)
Cross-linked polymer-blend gate dielectrics through thermal click chemistry
Chemistry?A European Journal , 21(49), 17762-17768 (2015)
One-step conversion of aldehydes to oxazolines and 5, 6-dihydro-4 H-1, 3-oxazines using 1, 2-and 1, 3-azido alcohols
The Journal of Organic Chemistry, 61, 2484-2487 (1996)
SPAAC-NAD-seq, a sensitive and accurate method to profile NAD+-capped transcripts
Proceedings of the National Academy of Sciences, 118, e2025595118-e2025595118 (2021)
1, 3-Dipolar and Diels-Alder cycloaddition reactions on polyester backbones possessing internal electron-deficient alkyne moieties
Polym. Chem., 7, 7094-7100 (2016)
1, 3-Dipolar and Diels-Alder cycloaddition reactions on polyester backbones possessing internal electron-deficient alkyne moieties
Polym. Chem., 7(46), 7094-7100 (2016)
商品
Explore the principles and applications of click chemistry in drug discovery, highlighting efficient reactions that streamline the synthesis of bioactive compounds.
Explore the principles and applications of click chemistry in drug discovery, highlighting efficient reactions that streamline the synthesis of bioactive compounds.
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