Dimethylthiocarbamoyl isopropylidene glucofuranose

Base Information

Chemical Name:Dimethylthiocarbamoyl isopropylidene glucofuranose
CAS No.:16713-76-1
Molecular Formula:C₁₅H₂₅NO₆S
Molecular Weight:347.433
Hs Code.:
NSC Number:98523
Mol file:16713-76-1.mol

Synonyms:NSC98523;16713-76-1;NSC-98523;Dimethylthiocarbamoyl isopropylidene glucofuranose;.alpha.-D-Glucofuranose,2:5,6-bis-O-(1-methylethylidene)-, dimethylcarbamothioate

Suppliers and Price of Dimethylthiocarbamoyl isopropylidene glucofuranose

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 3 raw suppliers

Chemical Property of Dimethylthiocarbamoyl isopropylidene glucofuranose

Chemical Property:

Vapor Pressure:2.09E-06mmHg at 25°C
Boiling Point:393.7°Cat760mmHg
Flash Point:191.9°C
Density:1.27g/cm³
XLogP3:1.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:3
Exact Mass:347.14025869
Heavy Atom Count:23
Complexity:483

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(OCC(O1)C2C(C3C(O2)OC(O3)(C)C)OC(=S)N(C)C)C

Technology Process of Dimethylthiocarbamoyl isopropylidene glucofuranose

There total 1 articles about Dimethylthiocarbamoyl isopropylidene glucofuranose 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:

: 350255-13-9
1,2:5,6-di-O-isopropylidene-α-D-glucofuranose

: 33842-02-3,529510-96-1
dichloromethylenedimethyliminium chloride

: 4239-73-0
Bis-<1.2:5.6-di-O-isopropyliden-α-D-glucofuranose>-3.3'-thionocarbonat

: 84730-39-2
3-O-(N,N-dimethylcarbamoyl)-1,2:5,6-di-O-isopropylidene-α-D-glucose

: 16713-76-1
Dimethyl-thiocarbamic acid O-[(3aR,5R,6S,6aR)-5-(2,2-dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl] ester

: 4239-74-1
bis(1,2;5,6-di-O-isopropylidene-α-D-glucosyl)carbonate

Guidance literature:: With sodium hydrogensulfide; triethylamine; Yield given. Multistep reaction; 1.) CH₂Cl₂, 25 deg C, 30 min, 2.) CH₂Cl₂, reflux, 20 h;