D-Xylono-1,5-lactone

Base Information

Chemical Name:D-Xylono-1,5-lactone
CAS No.:82796-87-0
Molecular Formula:C₅H₈O₅
Molecular Weight:148.116
Hs Code.:
UNII:RX4Z3X5JKZ
DSSTox Substance ID:DTXSID001345691
Nikkaji Number:J2.735.715F
Wikidata:Q27098270
Metabolomics Workbench ID:41464

Synonyms:D-Xylono-1,5-lactone;D-Xylonolactone;82796-87-0;(3R,4S,5R)-3,4,5-trihydroxyoxan-2-one;Xylonolactone;xylonolactone NIST;RX4Z3X5JKZ;D-Xylonic acid, delta-lactone;SCHEMBL2466054;CHEBI:15867;DTXSID001345691;C02266;(3R,4S,5R)-3,4,5-Tris(oxidanyl)oxan-2-one;Q27098270;(3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-one

Suppliers and Price of D-Xylono-1,5-lactone

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

Total 0 raw suppliers

Chemical Property of D-Xylono-1,5-lactone

Chemical Property:

XLogP3:-2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:0
Exact Mass:148.03717335
Heavy Atom Count:10
Complexity:145

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C(C(C(C(=O)O1)O)O)O
Isomeric SMILES:C1[C@H]([C@@H]([C@H](C(=O)O1)O)O)O

Technology Process of D-Xylono-1,5-lactone

There total 1 articles about D-Xylono-1,5-lactone 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:

: 15384-37-9
D-xylono-1,4-lactone

: 488-30-2,526-91-0,526-92-1,608-53-7,642-98-8,4172-43-4,4172-44-5,13171-74-9,13752-83-5,17812-24-7,17828-56-7,20663-19-8,28223-40-7
D-xylonic acid

D-xylono-1,5-lactone: 82796-87-0
D-xylono-1,5-lactone

Guidance literature:: With hydrogenchloride; In water-d2; at 22 ℃; for 44h; Mechanism; Product distribution; other pentalactones and their acetals and ketals;
DOI:10.1016/S0957-4166(00)80400-0

Reference yield: 80.0%

: 999-97-3
1,1,1,3,3,3-hexamethyl-disilazane

D-xylono-1,5-lactone: 82796-87-0
D-xylono-1,5-lactone

: 32384-59-1
C₁₄H₃₂O₅Si₃

Guidance literature:: With iodine; In dichloromethane; at 15 - 30 ℃; for 4h; Solvent; Temperature; Reagent/catalyst;

Reference yield:

D-xylono-1,5-lactone: 82796-87-0
D-xylono-1,5-lactone

: 41294-56-8
1α-hydroxyvitamin D3

Guidance literature:: Multi-step reaction with 14 steps

1: acetic acid / 50 °C

2: 97 percent / H₂, Et₃N / Pd/C / ethyl acetate / Ambient temperature

3: 90 percent / KOH, H₂O / ethanol / Ambient temperature

4: 95 percent / imidazole / dimethylformamide / Ambient temperature

5: 97 percent / (iPr)2NEt / CH₂Cl₂ / Ambient temperature

6: 97 percent / DIBAL / CH₂Cl₂ / -65 °C

7: 65 percent / tBuOK / tetrahydrofuran / 0 °C

8: 97 percent / (nBu)4NF / tetrahydrofuran / Ambient temperature

9: 74 percent / pyridine / -5 °C

10: 95 percent / K₂CO₃ / ethanol / Ambient temperature

11: 95 percent / dimethylsulfoxide / Ambient temperature

12: 97 percent / (iPr)2NEt / CH₂Cl₂ / Ambient temperature

13: 51 percent / (dba)3Pd₂*CHCl₃

14: 91 percent / ZnBr₂ / CH₂Cl₂

With pyridine; 1H-imidazole; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; potassium hydroxide; potassium tert-butylate; tetrabutyl ammonium fluoride; water; hydrogen; diisobutylaluminium hydride; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; zinc dibromide; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; acetic acid; dimethyl sulfoxide; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1016/0040-4039(94)02209-T