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Merck
CN

01510

1-O-乙酰基-2,3,5-O-三苯甲酰基-β-D-呋喃核糖

purum, ≥97.0% (TLC)

别名:

1-乙酰基-2,3,5-三苯甲酰基-β-D-呋喃核糖

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关于此项目

经验公式(希尔记法):
C28H24O9
化学文摘社编号:
分子量:
504.48
EC Number:
230-220-4
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
100243
MDL number:
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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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
841620025004022536884653
C105805-25G04061833460627
PHR2898-3X1.2ML04065266458633
841620005004022536647005
1154605-2X1ML04061837842696
C105805-100G04061833460610
C105805-5G04061833460634

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