1,2,3,4-Tetra-O-acetyl-alpha-D-xylopyranose

Base Information Edit

Chemical Name:1,2,3,4-Tetra-O-acetyl-alpha-D-xylopyranose
CAS No.:1233-03-0
Molecular Formula:C₁₃H₁₈O₉
Molecular Weight:318.281
Hs Code.:
DSSTox Substance ID:DTXSID20512675
Nikkaji Number:J119.588C
Mol file:1233-03-0.mol

Synonyms:1233-03-0;1,2,3,4-Tetra-O-acetyl-alpha-D-xylopyranose;.ALPHA.-XYLOPYRANOSE, TETRAACETATE;[(3R,4S,5R,6R)-4,5,6-triacetyloxyoxan-3-yl] acetate;4257-98-1;1,2,3,4-Tetra-O-acetylpentopyranose #;.alpha.-D-Xylopyranose, tetraacetate;Xylopyranose, tetraacetate, .alpha.-D-;SCHEMBL5350100;DTXSID20512675;MJOQJPYNENPSSS-YVECIDJPSA-N;Alpha-XYLOPYRANOSE TETRAACETATE;MFCD09864646;(2R,3R,4S,5R)-Tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate

Suppliers and Price of 1,2,3,4-Tetra-O-acetyl-alpha-D-xylopyranose

Supply Marketing:Edit

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

Total 6 raw suppliers

Chemical Property of 1,2,3,4-Tetra-O-acetyl-alpha-D-xylopyranose Edit

Chemical Property:

Melting Point:57-59 °C
Boiling Point:362.9±42.0 °C(Predicted)
PSA：114.43000
Density:1.29±0.1 g/cm3(Predicted)
LogP:-0.29910
XLogP3:-0.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:8
Exact Mass:318.09508215
Heavy Atom Count:22
Complexity:458

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OC1COC(C(C1OC(=O)C)OC(=O)C)OC(=O)C
Isomeric SMILES:CC(=O)O[C@@H]1CO[C@@H]([C@@H]([C@H]1OC(=O)C)OC(=O)C)OC(=O)C

Technology Process of 1,2,3,4-Tetra-O-acetyl-alpha-D-xylopyranose

There total 51 articles about 1,2,3,4-Tetra-O-acetyl-alpha-D-xylopyranose 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: 100.0%

: 87-72-9,608-45-7,608-46-8,608-47-9,2460-44-8,6748-95-4,6763-34-4,7261-26-9,7283-06-9,7283-07-0,7296-55-1,7296-56-2,7296-58-4,7296-59-5,7296-60-8,7296-61-9,7296-62-0,7322-30-7,10257-31-5,10257-32-6,10257-33-7,10257-34-8,10257-35-9,19982-83-3,20242-88-0,28697-53-2,36562-42-2,41546-41-2,89299-64-9,107655-34-5,115794-06-4,115794-07-5,130550-15-1,130606-21-2
L-(+)-arabinose

: 108-24-7
acetic anhydride

: 1233-03-0,2595-11-1,4026-34-0,4049-33-6,4049-34-7,4257-95-8,4257-98-1,4258-00-8,4627-30-9,17080-99-8,19186-37-9,25227-11-6,25243-38-3,62446-93-9,62929-49-1,67226-03-3,78087-60-2,78088-17-2,82890-16-2,86782-34-5,86782-35-6,92218-63-8,99880-95-2,108646-05-5,115939-79-2,142130-89-0,123163-97-3
1,2,3,4-tetra-O-acetyl-L-arabinopyranose

Guidance literature:: With pyridine; dmap; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1016/j.bmc.2003.12.034

Reference yield: 100.0%

: 6763-34-4
D-xylose

: 108-24-7
acetic anhydride

: 1233-03-0,2595-11-1,4026-34-0,4049-33-6,4049-34-7,4257-95-8,4257-98-1,4258-00-8,4627-30-9,17080-99-8,19186-37-9,25227-11-6,25243-38-3,62446-93-9,62929-49-1,67226-03-3,78087-60-2,78088-17-2,82890-16-2,86782-34-5,86782-35-6,92218-63-8,99880-95-2,108646-05-5,115939-79-2,123163-97-3,142130-89-0
α-D-xylopyranose tetraacetate

Guidance literature:: D-xylose; With dmap; triethylamine; In dichloromethane; at 0 - 25 ℃; for 0.166667h; Inert atmosphere;

acetic anhydride; In dichloromethane; at 0 - 25 ℃; for 1h; stereoselective reaction; Inert atmosphere;
DOI:10.1016/j.carres.2017.03.008