Dodecyl 1-thio-beta-D-glucopyranoside

Base Information

Chemical Name:Dodecyl 1-thio-beta-D-glucopyranoside
CAS No.:85618-22-0
Molecular Formula:C18H36O5S
Molecular Weight:348.47484
Hs Code.:
DSSTox Substance ID:DTXSID701296984
Nikkaji Number:J1.764.803I
Mol file:85618-22-0.mol

Synonyms:Dodecyl 1-thio-beta-D-glucopyranoside;SCHEMBL2989790;DTXSID701296984

Suppliers and Price of Dodecyl 1-thio-beta-D-glucopyranoside

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 1 raw suppliers

Chemical Property of Dodecyl 1-thio-beta-D-glucopyranoside

Chemical Property:

PSA：115.45000
LogP:2.44040
XLogP3:4.3
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:13
Exact Mass:364.22834542
Heavy Atom Count:24
Complexity:305

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCCSC1C(C(C(C(O1)CO)O)O)O
Isomeric SMILES:CCCCCCCCCCCCS[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O

Technology Process of Dodecyl 1-thio-beta-D-glucopyranoside

There total 7 articles about Dodecyl 1-thio-beta-D-glucopyranoside 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: 79.0%

: 85618-27-5
n-dodecyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside

: 85618-22-0
S-dodecyl 1-thio-β-D-glucopyranoside

Guidance literature:: With methanol; sodium methylate; at 20 ℃; for 16h;
DOI:10.1016/j.carres.2019.107905

Reference yield:

: 112-55-0
1-dodecylthiol

: 85618-22-0
S-dodecyl 1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / BF₃*Et₂O / 1,2-dichloro-ethane / 0.5 h / 20 °C

With boron trifluoride diethyl etherate; In 1,2-dichloro-ethane; 1: Substitution / 2: Deacetylation;
DOI:10.1246/cl.2000.326

Reference yield:

: 83-87-4,604-68-2,604-69-3,2152-77-4,4026-35-1,4163-59-1,4163-60-4,4163-61-5,4163-65-9,4257-94-7,4257-96-9,16299-15-3,19186-39-1,19189-55-0,25878-60-8,25941-03-1,32445-48-0,32445-49-1,32445-53-7,32445-54-8,34685-58-0,34685-59-1,43168-42-9,43168-44-1,43169-22-8,43169-25-1,66966-07-2,70749-17-6,80184-01-6,93221-01-3,93221-02-4,99630-88-3,109215-53-4,115792-70-6,115792-73-9,139894-92-1,139973-25-4,144071-49-8,147648-81-5
D-glucose pentaacetate

: 85618-22-0
S-dodecyl 1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: boron trifluoride diethyl etherate / 1,2-dichloro-ethane / 5 h / 20 °C

2: sodium methylate; methanol / 16 h / 20 °C

With methanol; boron trifluoride diethyl etherate; sodium methylate; In 1,2-dichloro-ethane;
DOI:10.1016/j.carres.2019.107905