2-Deoxy-D-ribose 1,3,4-Triacetate

Base Information

Chemical Name:2-Deoxy-D-ribose 1,3,4-Triacetate
CAS No.:4258-01-9
Molecular Formula:C₁₁H₁₆O₇
Molecular Weight:260.244
Hs Code.:
DSSTox Substance ID:DTXSID80431878
Nikkaji Number:J789.864I
Wikidata:Q82245886
Mol file:4258-01-9.mol

Synonyms:2-Deoxy-D-ribose 1,3,4-Triacetate;4258-01-9;[(2S,4S,5R)-2,5-diacetyloxyoxan-4-yl] acetate;(2S,4S,5R)-tetrahydro-2H-pyran-2,4,5-triyl triacetate;tetrahydro-2H-pyran-2,4,5-triyl triacetate;DTXSID80431878;AKOS032945222;CS-0180888;2-Deoxy-ss-D-erythro-pentopyranose Triacetate;1-O,3-O,4-O-Triacetyl-2-deoxy-beta-D-ribopyranose;-D-erythro-Pentopyranose, 2-deoxy-, 1,3,4-triacetate

Suppliers and Price of 2-Deoxy-D-ribose 1,3,4-Triacetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Usbiological
2-Deoxy-D-ribose 1,3,4-Triacetate
1g
$ 460.00

TRC
2-Deoxy-D-ribose1,3,4-Triacetate
10g
$ 1320.00

Total 7 raw suppliers

Chemical Property of 2-Deoxy-D-ribose 1,3,4-Triacetate

Chemical Property:

Storage Temp.:Refrigerator
Solubility.:Chloroform, Toluene
XLogP3:0.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:6
Exact Mass:260.08960285
Heavy Atom Count:18
Complexity:338

Purity/Quality:

99.90% ^*data from raw suppliers

2-Deoxy-D-ribose 1,3,4-Triacetate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OC1CC(OCC1OC(=O)C)OC(=O)C
Isomeric SMILES:CC(=O)O[C@H]1C[C@@H](OC[C@H]1OC(=O)C)OC(=O)C
Uses Protected 2-Deoxy-D-ribose (D252000). Induces apoptosis by inhibiting the synthesis and increasing the efflux of glutathione.

Technology Process of 2-Deoxy-D-ribose 1,3,4-Triacetate

There total 1 articles about 2-Deoxy-D-ribose 1,3,4-Triacetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 93.0%

: Acetic acid (2R,3S,4R,5R)-4,5-diacetoxy-2-(2,2-dimethyl-propoxythiocarbonylsulfanyl)-tetrahydro-pyran-3-yl ester

: Dithiocarbonic acid S-cyclohexyl ester O-(2,2-dimethyl-propyl) ester

: 4258-01-9
1,3,4-tri-O-acetyl-2-deoxy-β-D-erythro-pentopyranose

Guidance literature:: With dilauryl peroxide; cyclohexane; Heating;
DOI:10.1021/ja9619622

Reference yield:

: 4258-01-9
1,3,4-tri-O-acetyl-2-deoxy-β-D-erythro-pentopyranose

: 110267-81-7
Amrubicin

Guidance literature:: Multi-step reaction with 4 steps

1: ammonia / tetrahydrofuran; methanol / 1 h / 0 - 20 °C

2: 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 2 h / 0 - 20 °C

3: trimethylsilyl trifluoromethanesulfonate / dichloromethane; diethyl ether / 4 h / -10 - 20 °C

4: potassium carbonate / dichloromethane; methanol / 16 h / 0 - 5 °C

With trimethylsilyl trifluoromethanesulfonate; ammonia; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; methanol; diethyl ether; dichloromethane;