所有图片(1)
About This Item
经验公式(希尔记法):
C14H28N2O4S
CAS号:
分子量:
320.45
Beilstein:
9559826
MDL编号:
UNSPSC代码:
12352108
eCl@ss:
32110502
PubChem化学物质编号:
NACRES:
NA.22
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方案
≥99.0% (HPLC)
mp
98-100 °C
应用
peptide synthesis
SMILES字符串
CC(C)(C)OC(=O)NN(SC(C)(C)C)C(=O)OC(C)(C)C
InChI
1S/C14H28N2O4S/c1-12(2,3)19-10(17)15-16(21-14(7,8)9)11(18)20-13(4,5)6/h1-9H3,(H,15,17)
InChI key
MOWYOPQOADUFLA-UHFFFAOYSA-N
其他说明
用于在有机溶液中制备非对称性 S-叔丁基二硫化物衍生物(例如向半胱氨酸多肽引入 S-叔丁基硫代保护基团)的稳定试剂
储存分类代码
13 - Non 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)
E Wünsch et al.
Hoppe-Seyler's Zeitschrift fur physiologische Chemie, 363(12), 1461-1464 (1982-12-01)
The sterically hindered tert-butyl thiol reacts smoothly with azodicarboxylic acid derivatives only upon addition of catalytic amounts of sodium alcoholate, yielding crystalline and analytically well characterized 1-(tert-butylthio)-1,2-hydrazinedicarboxylic acid derivatives. These sulfur-activated reagents were found to be stable on storage and
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