712620
N-Boc-4-叠氮-L-高丙氨酸 二环己基铵盐
≥97% (CE)
别名:
(S)-4-叠氮-2-(Boc-氨基)丁酸 二环己基铵盐
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关于此项目
经验公式（希尔记法）:
C21H39N5O4
化学文摘社编号:
分子量:
425.57
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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
SMILES string
C1CCC(CC1)NC2CCCCC2.CC(C)(C)OC(=O)N[C@@H](CCN=[N+]=[N-])C(O)=O
InChI key
UCLAYMPJMDBLOX-ZCMDIHMWSA-N
assay
≥97% (CE)
form
crystals
optical activity
[α]/D +15.5±1.0°, c = 1 in ethanol
composition
carbon, 57.5-61.0% , nitrogen, 16.0-16.9%
reaction suitability
reaction type: click chemistry
application(s)
peptide synthesis
storage temp.
2-8°C
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
A James Link et al.
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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