09440
(R)-(+)-四氢-3-呋喃基胺 对甲苯磺酸盐
≥99.0% (T)
别名:
(R)-(+)-3-氨基四氢呋喃 对甲苯磺酸盐
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关于此项目
经验公式（希尔记法）:
C4H9NO · C7H8O3S
化学文摘社编号:
分子量:
259.32
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5783386
Quality Level
assay
≥99.0% (T)
optical activity
[α]20/D +4.5±0.5°, c = 3% in methanol
mp
139-141 °C
functional group
ether, tosylate
SMILES string
N[C@@H]1CCOC1.Cc2ccc(cc2)S(O)(=O)=O
InChI
1S/C7H8O3S.C4H9NO/c1-6-2-4-7(5-3-6)11(8,9)10;5-4-1-2-6-3-4/h2-5H,1H3,(H,8,9,10);4H,1-3,5H2/t;4-/m.1/s1
InChI key
BZXPLADBSZWDIH-FZSMXKCYSA-N
Other Notes
手性胺；可与氨基酸发生酰胺化
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
K. Barlos et al.
Liebigs Ann. Chem., 1950-1950 (1986)
Glorymar Ibanez et al.
Combinatorial chemistry & high throughput screening, 15(5), 359-371 (2012-01-20)
Protein methyltransferases (PMTs) orchestrate epigenetic modifications through post-translational methylation of various protein substrates including histones. Since dysregulation of this process is widely implicated in many cancers, it is of pertinent interest to screen inhibitors of PMTs, as they offer novel
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 42438-50MG | 04061832103693 |
| 36927-250MG | 04061831833027 |
| 308501-5ML | 04061826674758 |
| 308501-1L | 04061837812187 |
| 308501-250ML | 04061826674734 |
| 442503 | 04061838080936 |
| 09440-1G | 04061834411024 |
| 09440-250MG | 04061832985237 |
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