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关于此项目
经验公式(希尔记法):
C3H7N3O
化学文摘社编号:
分子量:
101.11
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352125
MDL number:
产品名称
3-叠氮基-1-丙醇, ≥96%
InChI
1S/C3H7N3O/c4-6-5-2-1-3-7/h7H,1-3H2
SMILES string
OCCCN=[N+]=[N-]
InChI key
WHVSIWLMCCGHFW-UHFFFAOYSA-N
assay
≥96%
form
liquid
reaction suitability
reaction type: click chemistry
refractive index
n20/D 1.461
density
1.095 g/mL at 25 °C
storage temp.
2-8°C
Quality Level
Application
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
General description
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。
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Proceedings of the National Academy of Sciences, 118, e2025595118-e2025595118 (2021)
One-step conversion of aldehydes to oxazolines and 5, 6-dihydro-4 H-1, 3-oxazines using 1, 2-and 1, 3-azido alcohols
JG Badiang, et al.
The Journal of Organic Chemistry, 61, 2484-2487 (1996)
Cross-linked polymer-blend gate dielectrics through thermal click chemistry
Li S, et al.
Chemistry?A European Journal , 21(49), 17762-17768 (2015)
1, 3-Dipolar and Diels-Alder cycloaddition reactions on polyester backbones possessing internal electron-deficient alkyne moieties
Cetin M, et al.
Polym. Chem., 7(46), 7094-7100 (2016)
1, 3-Dipolar and Diels-Alder cycloaddition reactions on polyester backbones possessing internal electron-deficient alkyne moieties
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商品
Explore click chemistry: efficient, high-yield reactions for drug discovery, bioconjugation, and green chemistry with simple conditions and wide applications.
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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