Acetobromo-alpha-maltose

Base Information

Chemical Name:Acetobromo-alpha-maltose
CAS No.:68682-05-3
Molecular Formula:C₂₆H₃₅BrO₁₇
Molecular Weight:699.458
Hs Code.:
European Community (EC) Number:634-315-5
DSSTox Substance ID:DTXSID00515407
Nikkaji Number:J1.616.667G
Wikidata:Q72434234

Synonyms:acetobromo-alpha-maltose;14257-35-3;[(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-[(2R,3R,4S,5R,6S)-4,5-diacetyloxy-2-(acetyloxymethyl)-6-bromooxan-3-yl]oxyoxan-2-yl]methyl acetate;acetobromomaltose;SCHEMBL8109741;DTXSID00515407;AKOS032950051;(2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-((2R,3R,4S,5R,6S)-4,5-diacetoxy-2-(acetoxymethyl)-6-bromotetrahydro-2H-pyran-3-yloxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate;2,3,6-Tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-alpha-D-glucopyranosyl)-beta-D-glucopyranosyl bromide

Suppliers and Price of Acetobromo-alpha-maltose

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Acetobromo-alpha-maltose

Chemical Property:

XLogP3:0.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:17
Rotatable Bond Count:18
Exact Mass:698.10576
Heavy Atom Count:44
Complexity:1090

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)OCC1C(C(C(C(O1)OC2C(OC(C(C2OC(=O)C)OC(=O)C)Br)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C
Isomeric SMILES:CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2OC(=O)C)OC(=O)C)Br)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C

Technology Process of Acetobromo-alpha-maltose

There total 19 articles about Acetobromo-alpha-maltose 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: 100.0%

: 22352-19-8
2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl-(1->4)-2,3,6-tri-O-acetyl-β-D-glucopyranosyl acetate

: 4753-07-5,5160-10-1,14206-57-6,14227-66-8,14257-35-3,42385-75-1,67650-37-7,68682-05-3,69308-57-2,69349-74-2,70223-96-0,70223-97-1,71276-38-5,85248-99-3,118493-15-5,120575-76-0
2,3,6,2',3',4',6'-hepta-O-acetyl-α-D-maltosyl bromide

Guidance literature:: With hydrogen bromide; acetic acid; for 3h; Ambient temperature;
DOI:10.1021/jo00062a020

Reference yield: 95.1%

: 18464-08-9,66073-13-0,71623-44-4,101981-29-7,109922-72-7,109922-73-8,132287-75-3,132287-76-4,132287-78-6,132303-63-0,134311-82-3,134333-39-4
2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl-(1->4)-2,3,6-tri-O-acetyl-β-D-glucopyranose

: 70223-96-0,4753-07-5,5160-10-1,14206-57-6,14227-66-8,14257-35-3,42385-75-1,67650-37-7,68682-05-3,69308-57-2,69349-74-2,70223-97-1,71276-38-5,85248-99-3,118493-15-5,120575-76-0
2,2',3,3',4',6,6'-hepta-O-acetyl-β-D-cellobiosyl bromide

Guidance literature:: With hydrogen bromide; In chloroform; acetic acid; at 0 - 20 ℃;
DOI:10.1016/j.bmc.2013.12.062

Reference yield: 92.0%

: 18464-08-9,66073-13-0,71623-44-4,101981-29-7,109922-72-7,109922-73-8,132287-75-3,132287-76-4,132287-78-6,132303-63-0,134311-82-3,134333-39-4
2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-D-glucopyranose

: 4753-07-5,5160-10-1,14206-57-6,14227-66-8,14257-35-3,42385-75-1,67650-37-7,68682-05-3,69308-57-2,69349-74-2,70223-96-0,70223-97-1,71276-38-5,85248-99-3,118493-15-5,120575-76-0
2,3,6,2',3',4',6'-hepta-O-acetyl-α-D-maltosyl bromide

Guidance literature:: With tris(2,2'-bipyridyl)ruthenium dichloride; carbon tetrabromide; tetrabutylammomium bromide; In N,N-dimethyl-formamide; Schlenk technique; Sealed tube; Inert atmosphere; Irradiation;
DOI:10.1055/s-0033-1340493