Methyl 2-methylsulfonyl-alpha-d-xylofuranoside

Base Information

Chemical Name:Methyl 2-methylsulfonyl-alpha-d-xylofuranoside
CAS No.:53081-34-8
Molecular Formula:C₇H₁₄O₇S
Molecular Weight:242.25
Hs Code.:
NSC Number:106760
DSSTox Substance ID:DTXSID10967594

Synonyms:53081-34-8;NSC106760;DTXSID10967594;ZHAGGSCPZAPHFA-UHFFFAOYSA-N;NSC-106760;Methyl 2-O-(methanesulfonyl)pentofuranoside;Methyl 2-O-(methylsulfonyl)pentofuranoside #;Methyl 2-methylsulfonyl-.alpha.-d-xylofuranoside

Suppliers and Price of Methyl 2-methylsulfonyl-alpha-d-xylofuranoside

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 2 raw suppliers

Chemical Property of Methyl 2-methylsulfonyl-alpha-d-xylofuranoside

Chemical Property:

Vapor Pressure:1.12E-11mmHg at 25°C
Boiling Point:490.4°Cat760mmHg
Flash Point:250.4°C
Density:1.49g/cm³
XLogP3:-1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:4
Exact Mass:242.04602395
Heavy Atom Count:15
Complexity:295

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1C(C(C(O1)CO)O)OS(=O)(=O)C

Technology Process of Methyl 2-methylsulfonyl-alpha-d-xylofuranoside

There total 3 articles about Methyl 2-methylsulfonyl-alpha-d-xylofuranoside 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: 89.0%

: 7045-39-8
methyl 3,5-O-isopropylidene-2-O-mesyl-α-D-xylofuranoside

: 53081-34-8
methyl 2-O-mesyl-α-D-xylofuranoside

Guidance literature:: With acetyl chloride; In methanol; at 20 ℃; for 4h;
DOI:10.1016/j.carres.2004.04.020

Reference yield:

: 7045-40-1
Methyl 3,5-O-Isopropylidene-α-D-xylofuranoside

: 53081-34-8
methyl 2-O-mesyl-α-D-xylofuranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / NEt₃ / CH₂Cl₂ / -20 - 20 °C

2: 89 percent / acetyl chloride / methanol / 4 h / 20 °C

With triethylamine; acetyl chloride; In methanol; dichloromethane;
DOI:10.1016/j.carres.2004.04.020