439908
1,3-双(叔-丁氧基羰基)-2-甲基-2-硫代假脲
98%
别名:
N,N′-二-Boc-S-甲基异硫脲, 1,3-二-2-甲基异硫脲, N,N′-双(叔-丁氧羰基)-S-甲基异硫脲
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关于此项目
线性分子式:
(CH3)3CO2CN=C(SCH3)NHCO2C(CH3)3
化学文摘社编号:
分子量:
290.38
Beilstein:
5815984
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
98%
mp
115-121 °C (lit.)
应用
peptide synthesis
SMILES字符串
CS\C(NC(=O)OC(C)(C)C)=N/C(=O)OC(C)(C)C
InChI
1S/C12H22N2O4S/c1-11(2,3)17-9(15)13-8(19-7)14-10(16)18-12(4,5)6/h1-7H3,(H,13,14,15,16)
InChI key
UQJXXWHAJKRDKY-UHFFFAOYSA-N
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储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Liam Martin et al.
Biomacromolecules, 19(8), 3190-3200 (2018-06-12)
A range of well-defined guanidinium-rich linear polymers with demonstrable efficiency for cellular internalization were developed. A protected guanidinium-functional acrylamide monomer (di-Boc-guanidinium ethyl acrylamide, GEAdiBoc) was synthesized and then polymerized via RAFT polymerization to yield well-defined homopolymers, which were then deprotected
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