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Merck
CN

761540

二苯并环辛炔胺

for Copper-free Click Chemistry

别名:

DBCO-NH2, DBCO胺

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关于此项目

经验公式(希尔记法):
C18H16N2O
化学文摘社编号:
分子量:
276.33
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352116
MDL number:
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产品名称

二苯并环辛炔胺, for Copper-free Click Chemistry

InChI

1S/C18H16N2O/c19-12-11-18(21)20-13-16-7-2-1-5-14(16)9-10-15-6-3-4-8-17(15)20/h1-8H,11-13,19H2

SMILES string

NCCC(N1CC2=C(C=CC=C2)C#CC3=C1C=CC=C3)=O

InChI key

OCCYFTDHSHTFER-UHFFFAOYSA-N

assay

≥94.5 %

form

solid

reaction suitability

reaction type: click chemistry
reagent type: linker

mp

86-96 °C

functional group

amine

storage temp.

−20°C

Quality Level

Application

二苯并环辛炔胺可用作:
  • 连接含叠氮化物官能团的连接剂。它通过应变促进的叠氮化物-炔烃环加成反应(SPAAC)促进键的形成
  • 合成氮杂环卡宾金属硫醇盐的试剂。它使金属复合物官能化,增加应变促进的炔烃–叠氮化物环加成(SPAAC) 反应的反应活性
  • 胺官能化环辛炔衍生物。环辛炔可用于菌株促进的无铜叠氮化物-炔烃环加成反应。该二苯并环辛炔可在不需要Cu(I)催化剂的情况下,与叠氮官能化化合物或生物分子反应,以产生稳定的三唑键。

General description

二苯并环辛炔胺(DBCO-NH2) 是一种杂官能团连接剂,含有一个DBCO结构单元,该结构单元常用于纳米抗体(nanobodies )的位点特异性官能化,促进随后的点击化学反应中反应性DBCO基团的引入。

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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访问文档库

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V Somasundaram, et al.
Inorganic Chemistry, 57, 11184-11192 (2018)
Prolonging the circulatory retention of SPIONs using dextran sulfate: in vivo tracking achieved by functionalisation with near-infrared dyes.
Abdollah MR, et al.
Faraday Discussions, 175, 41-58 (2015)
Steering the azido?tetrazole equilibrium of 4-azidopyrimidines via substituent variation?implications for drug design and azide?alkyne cycloadditions.
Thomann A, et al.
Organic & Biomolecular Chemistry, 13(43), 10620-10630 (2015)
An azide functionalized oligothiophene ligand?A versatile tool for multimodal detection of disease associated protein aggregates.
Johansson LB, et al.
Biosensors And Bioelectronics, 63, 204-211 (2015)
Covalently linking CuInS 2 quantum dots with a Re catalyst by click reaction for photocatalytic CO 2 reduction
J Huang, et al.
Dalton Transactions, 47, 10775-10783 (2018)

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.

Copper-free click chemistry is an alternative approach to click chemistry that proceeds at a lower activation barrier and is free of cytotoxic transition metal catalysts.

无铜点击化学是点击化学的一种替代方法,可在较低的活化屏障下进行,且没有细胞毒性过渡金属催化剂。

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