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745073

N-[（1R,8S,9s）-双环[6.1.0]壬-4-炔-9-基甲氧基羰基]-1,8-二氨基-3,6-二氧杂辛烷

for Copper-free Click Chemistry

别名:

（1α,8α,9β）-双环[6.1.0] N- {2-[2-（2-氨基乙氧基）乙氧基]乙基}氨基甲酸酯非-4-炔-9-基甲基酯

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关于此项目

经验公式（希尔记法）:
C17H28N2O4
化学文摘社编号:
1263166-93-3
分子量:
324.42
NACRES:
NA.22
PubChem Substance ID:
329765726
UNSPSC Code:
12352003
MDL number:
MFCD19705418
Form:
liquid
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Quality Level

100

form

liquid

composition

carbon content, 62.94% , hydrogen content, 8.70% , nitrogen content, 8.63%

reaction suitability

reaction type: click chemistry, reagent type: linker

solubility

water: 1.5 g/L

density

1.14  g/cm3 at 20  °C

functional group

amine

shipped in

dry ice

storage temp.

−20°C

SMILES string

[H][C@@]12CCC#CCC[C@]1([H])[C@@H]2COC(NCCOCCOCCN)=O

InChI

1S/C17H28N2O4/c18-7-9-21-11-12-22-10-8-19-17(20)23-13-16-14-5-3-1-2-4-6-15(14)16/h14-16H,3-13,18H2,(H,19,20)/t14-,15+,16-

InChI key

YZGOWXGENSKDSE-MUJYYYPQSA-N

Application

N-[（1R,8S,9s）-双环[6.1.0]壬-4-炔-9-甲氧基羰基] -1,8-二氨基-3,6-二氧杂辛烷可用于双环[6.1.0]壬烯（BCN）功能化透明质酸，用于开发具有可调性质的响应性 HA 基物理水凝胶。
胺官能化的环辛炔衍生物。环辛炔可用于应变促进的无铜叠氮化物-炔烃环加成反应。该应变环辛炔将与叠氮官能化化合物或生物分子反应，无需铜催化剂即可产生稳定的三唑键。

Packaging

无底玻璃瓶。内含物装在插入的融合锥内。

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCN7535
BCCL6140
BCCK8171
BCCJ9740
BCCH9737

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商品

Click Chemistry in Drug Discovery

Explore the principles and applications of click chemistry in drug discovery, highlighting efficient reactions that streamline the synthesis of bioactive compounds.

Click Chemistry in Drug Discovery

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

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.

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全球贸易项目编号

货号GTIN
745073-100MG04061832889436
745073-25MG04061833441039