6-Chloro-6-deoxy-alpha-d-glucopyranose

Base Information

Chemical Name:6-Chloro-6-deoxy-alpha-d-glucopyranose
CAS No.:28528-86-1
Molecular Formula:C6H11 Cl O5
Molecular Weight:198.603
Hs Code.:2932999099
UNII:V9ZDE5M64V
Nikkaji Number:J911.603F
Mol file:28528-86-1.mol

Synonyms:28528-86-1;6-Chloro-6-deoxy-alpha-d-glucopyranose;(2S,3R,4S,5S,6S)-6-(chloromethyl)oxane-2,3,4,5-tetrol;V9ZDE5M64V;alpha-D-Glucopyranose, 6-chloro-6-deoxy-;6-Chloro-6-deoxy-a-d-glucopyranose;UNII-V9ZDE5M64V;SCHEMBL3147526;(2S,3R,4S,5S,6S)-6-(Chloromethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol;AKOS006281048;6-CHLORO-6-DEOXY-.ALPHA.-D-GLUCOPYRANOSE;.ALPHA.-D-GLUCOPYRANOSE, 6-CHLORO-6-DEOXY-;(2S, 3R, 4S, 5S, 6S)-6-(chloromethyl)oxane-2, 3, 4, 5-tetrol

Suppliers and Price of 6-Chloro-6-deoxy-alpha-d-glucopyranose

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

TRC
6-Chloro-6-deoxy-α-D-glucopyranose
50mg
$ 180.00

Medical Isotopes, Inc.
6-Chloro-6-deoxy-α-D-glucopyranose
50 mg
$ 475.00

Medical Isotopes, Inc.
6-Chloro-6-deoxy-α-D-glucopyranose
250 mg
$ 1275.00

American Custom Chemicals Corporation
6-CHLORO-6-DEOXY-ALPHA-D-GLUCOPYRANOSE 95.00%
5MG
$ 502.40

Total 6 raw suppliers

Chemical Property of 6-Chloro-6-deoxy-alpha-d-glucopyranose

Chemical Property:

PSA：90.15000
LogP:-1.97490
Storage Temp.:Hygroscopic, -20°C Freezer, Under inert atmosphere
Solubility.:Methanol (Slightly), Water (Slightly)
XLogP3:-1.9
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:198.0295011
Heavy Atom Count:12
Complexity:155

Purity/Quality:

99%, ^*data from raw suppliers

6-Chloro-6-deoxy-α-D-glucopyranose ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(C1C(C(C(C(O1)O)O)O)O)Cl
Isomeric SMILES:C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O)O)O)O)Cl
Uses 6-Chloro-6-deoxy-α-D-glucopyranose is a reactant used in the synthesis of 6-chloro-6-deoxy-1,2,3,4-tetra-O-galloyl-α-D-glucopyranose which may be used as an antidiabetic.

Technology Process of 6-Chloro-6-deoxy-alpha-d-glucopyranose

There total 9 articles about 6-Chloro-6-deoxy-alpha-d-glucopyranose 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:

: 57569-50-3
6-chloro-6-deoxy-1,2-O-(1-methylethylidene)-α-D-glucofuranose

: 14218-19-0,18961-69-8,28528-86-1,56688-73-4,68510-58-7
6-chloro-6-deoxyglucose

Guidance literature:: With Amberlite IR-120 (H⁽¹⁺⁾) resin; In water; at 100 ℃; for 0.5h;
DOI:10.1016/0008-6215(83)88169-5

Reference yield:

: 40984-16-5
6,6'-dichloro-6,6'-didesoxysaccharose

: 14218-19-0,18961-69-8,28528-86-1,56688-73-4,68510-58-7
6-chloro-6-deoxyglucose

: C₁₂H₁₈Cl₂O₈

: 151427-75-7
6-chloro-6-deoxy-α-D-fructofuranose 6-chloro-6-deoxy-β-D-fructofuranose 1,2':2,1'-dianhydride

: (2S,3S,4S,5R,8R,10S,11S,12S)-2,10-Bis-chloromethyl-1,6,9,13-tetraoxa-dispiro[4.2.4.2]tetradecane-3,4,11,12-tetraol

Guidance literature:: With pyridine hydrogenfluoride; at 20 ℃; for 0.333333h; Further byproducts given;
DOI:10.1016/0008-6215(94)00239-8

Reference yield:

: 57569-47-8
6-chloro-6-deoxy-1,2-O-isopropylidene-α-D-glucofuranose 3,5-bis(chlorosulfate)

: 14218-19-0,18961-69-8,28528-86-1,56688-73-4,68510-58-7
6-chloro-6-deoxyglucose

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / methanolic 10percent sodium iodide, sodium hydrogencarbonate / acetone; methanol

2: 0.42 g / Amberlite IR-120 (H⁽¹⁺⁾) resin / H₂O / 0.5 h / 100 °C

With Amberlite IR-120 (H⁽¹⁺⁾) resin; sodium hydrogencarbonate; sodium iodide; In methanol; water; acetone;
DOI:10.1016/0008-6215(83)88169-5