94624
S-(1-氧代-2-吡啶基)-N,N,N′,N′-四甲基硫脲六氟磷酸盐
≥95.0% (NMR)
别名:
N,N,N′,N′-四甲基-S-(1-氧代-2-吡啶基)硫脲六氟磷酸盐, S-(2-吡啶基)-N,N,N′,N′-四甲基硫脲 N-氧化物六氟磷酸盐
选择尺寸
About This Item
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方案
≥95.0% (NMR)
表单
crystals
反应适用性
reaction type: Coupling Reactions
mp
120-125 °C
应用
peptide synthesis
官能团
amine
thiourea
储存温度
−20°C
SMILES字符串
F[P-](F)(F)(F)(F)F.CN(C)\C(=[S+]\c1cccc[n+]1[O-])N(C)C
InChI
1S/C10H16N3OS.F6P/c1-11(2)10(12(3)4)15-9-7-5-6-8-13(9)14;1-7(2,3,4,5)6/h5-8H,1-4H3;/q+1;-1
InChI key
UCOGEMMJHLHOAW-UHFFFAOYSA-N
1 of 4
此商品 | 85971 | 23955 | M043100 |
---|---|---|---|
assay ≥95.0% (NMR) | assay ≥98.0% (CHN) | assay ≥97.5% (CHN) | assay ≥97% (31P-NMR), ≥97.0% (reversed phase HPLC) |
storage temp. −20°C | storage temp. 2-8°C | storage temp. 2-8°C | storage temp. −20°C |
mp 120-125 °C | mp 143-153 °C | mp 153-156 °C | mp - |
reaction suitability reaction type: Coupling Reactions | reaction suitability reaction type: Coupling Reactions | reaction suitability reaction type: Coupling Reactions | reaction suitability - |
application(s) peptide synthesis | application(s) peptide synthesis | application(s) peptide synthesis | application(s) - |
应用
Synthesis of inhibitors for PAD1, 3, and 4
Synthesis of enantiomerically pure vinylcyclopropylboronic esters
Synthesis of enantiomerically pure cyclopropane building blocks
Camphor-derived chiral auxiliary for hydroxyalkyl radicals
Solution and solid-phase coupling
Conversion of carboxylic acids to Weinreb amides and N-methoxy or N-benzoxy amides
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)
法规信息
历史批次信息供参考:
分析证书(COA)
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