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检测方案
≥97% (CE)
形式
crystals
旋光性
[α]/D +15.5±1.0°, c = 1 in ethanol
组成
carbon, 57.5-61.0%
nitrogen, 16.0-16.9%
反应适用性
reaction type: click chemistry
应用
peptide synthesis
储存温度
2-8°C
SMILES字符串
C1CCC(CC1)NC2CCCCC2.CC(C)(C)OC(=O)N[C@@H](CCN=[N+]=[N-])C(O)=O
InChI
1S/C12H23N.C9H16N4O4/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12;1-9(2,3)17-8(16)12-6(7(14)15)4-5-11-13-10/h11-13H,1-10H2;6H,4-5H2,1-3H3,(H,12,16)(H,14,15)/t;6-/m.0/s1
InChI key
UCLAYMPJMDBLOX-ZCMDIHMWSA-N
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
Journal of the American Chemical Society, 126(34), 10598-10602 (2004-08-26)
An improved protocol for copper-catalyzed triazole formation on the bacterial cell surface is described. Addition of highly pure CuBr to cells treated with azidohomoalanine (2) leads to ca. 10-fold more extensive cell surface labeling than previously observed. This highly active
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