grade
purum
assay
≥97.0% (TLC)
optical activity
[α]20/D +44±1°, c = 0.5% in chloroform
mp
128-130 °C
SMILES string
CC(=O)O[C@@H]1O[C@H](COC(=O)c2ccccc2)[C@@H](OC(=O)c3ccccc3)[C@H]1OC(=O)c4ccccc4
InChI
1S/C28H24O9/c1-18(29)34-28-24(37-27(32)21-15-9-4-10-16-21)23(36-26(31)20-13-7-3-8-14-20)22(35-28)17-33-25(30)19-11-5-2-6-12-19/h2-16,22-24,28H,17H2,1H3/t22-,23-,24-,28-/m1/s1
InChI key
GCZABPLTDYVJMP-CBUXHAPBSA-N
Other Notes
核糖衍生物,用于核苷的合成;与 Me3SiC 产生 1-氰化反应
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
涉药品监管产品
此项目有
M. Saneyoshi et al.
Chemical & Pharmaceutical Bulletin, 27, 2518-2518 (1979)
A. Matsuda et al.
Synthesis, 748-748 (1981)
K. Utimoto et al.
Tetrahedron Letters, 23, 237-237 (1982)
Z Tocik et al.
Nucleic acids research, 8(20), 4755-4761 (1980-10-24)
1-O-Acetyl-2,3,5-tri-O-benzoyl-beta-D-ribofuranose (I) was reacted with iodotrimethylsilane (II) and the product, the glycosyl iodide, was coupled with silylated uracil to afford 1-(2,3,5-tri-O-benzoyl-beta-D-ribofuranosyl)uracil (III; 89%), with silyated cytosine to afford, on subsequent acetylation, 1-(2,3,5-tri-O-benzoyl-beta-0D-ribofuranosyl)-4-acetamido-2-(1H)-pyrimidinone (IVb; 81%), and with chloromercuri-N-benzoyl-adenine to afford Va
A general synthesis of N-glycosides. I. Synthesis of pyrimidine nucleosides.
U Niedballa et al.
The Journal of organic chemistry, 39(25), 3654-3660 (1974-12-13)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 8416200250 | 04022536884653 |
| C105805-25G | 04061833460627 |
| PHR2898-3X1.2ML | 04065266458633 |
| 8416200050 | 04022536647005 |
| 1154605-2X1ML | 04061837842696 |
| C105805-100G | 04061833460610 |
| C105805-5G | 04061833460634 |
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