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5-Bromo-6-chloro-3-indoxyl-beta-D-glucopyranoside

Base Information Edit
  • Chemical Name:5-Bromo-6-chloro-3-indoxyl-beta-D-glucopyranoside
  • CAS No.:93863-89-9
  • Molecular Formula:C14H15BrClNO6
  • Molecular Weight:408.633
  • Hs Code.:29400090
  • DSSTox Substance ID:DTXSID101230382
  • Mol file:93863-89-9.mol
5-Bromo-6-chloro-3-indoxyl-beta-D-glucopyranoside

Synonyms:93863-89-9;5-Bromo-6-chloro-3-indoxyl-beta-D-glucopyranoside;5-Bromo-6-chloro-3-indolyl-beta-D-glucopyranoside;(2S,3R,4S,5S,6R)-2-((5-Bromo-6-chloro-1H-indol-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol;b-D-Glucopyranoside,5-bromo-6-chloro-1H-indol-3-yl;(2S,3R,4S,5S,6R)-2-[(5-BROMO-6-CHLORO-1H-INDOL-3-YL)OXY]-6-(HYDROXYMETHYL)OXANE-3,4,5-TRIOL;5-Bromo-6-chloro-3-indolyl beta-D-glucopyranoside;5-Bromo-6-chloro-1H-indol-3-yl beta-D-glucopyranoside;Magenta-Glc;SCHEMBL174647;Magenta-Gal, reagent for selection of recombinant bacterial clones;DTXSID101230382;MFCD00210022;AKOS015919327;CS-W021017;AS-74854;B-7270;E84064;A859621;5-Bromo-6-chloro-3-indolyl- beta -D-glucopyranoside;5-Bromo-6-chloro-3-indolyl-beta-D-glucopyranoside, >=98.0% (TLC);(2S,3R,4S,5S,6R)-2-(5-bromo-6-chloro-1H-indol-3-yloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol;(2S,3R,4S,5S,6R)-2-[(5-Bromo-6-chloro-1H-indol-3-yl)oxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol

Suppliers and Price of 5-Bromo-6-chloro-3-indoxyl-beta-D-glucopyranoside
Supply Marketing:Edit
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
  • Usbiological
  • 5-Bromo-6-chloro-3-indolyl b-D-glucopyranoside
  • 1g
  • $ 360.00
  • Usbiological
  • 5-Bromo-6-chloro-3-indoxyl-b-D-glucopyranoside
  • 250mg
  • $ 252.00
  • TRC
  • 5-Bromo-6-chloro-3-indolylb-D-glucopyranoside
  • 100mg
  • $ 60.00
  • TRC
  • 5-Bromo-6-chloro-3-indolylb-D-glucopyranoside
  • 50mg
  • $ 45.00
  • Sigma-Aldrich
  • 5-Bromo-6-chloro-3-indolyl-β-D-glucopyranoside ≥98.0% (TLC)
  • 100mg
  • $ 28.70
  • Sigma-Aldrich
  • 5-Bromo-6-chloro-3-indolyl-β-D-glucopyranoside ≥98.0% (TLC)
  • 500mg
  • $ 116.00
  • Iris Biotech GmbH
  • Magenta-beta-D-Glc
  • 2,5 g
  • $ 364.50
  • Iris Biotech GmbH
  • Magenta-beta-D-Glc
  • 25 g
  • $ 1930.50
  • Iris Biotech GmbH
  • Magenta-beta-D-Glc
  • 1 g
  • $ 256.50
  • Iris Biotech GmbH
  • Magenta-beta-D-Glc
  • 5 g
  • $ 580.50
Total 29 raw suppliers
Chemical Property of 5-Bromo-6-chloro-3-indoxyl-beta-D-glucopyranoside Edit
Chemical Property:
  • Boiling Point:673.9 °C at 760 mmHg 
  • PKA:12.78±0.70(Predicted) 
  • Flash Point:361.3 °C 
  • PSA:115.17000 
  • Density:1.882 g/cm3 
  • LogP:0.76250 
  • Storage Temp.:2-8°C 
  • XLogP3:1.2
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:3
  • Exact Mass:406.97713
  • Heavy Atom Count:23
  • Complexity:421
Purity/Quality:

98% *data from raw suppliers

5-Bromo-6-chloro-3-indolyl b-D-glucopyranoside *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements: 22-24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=C2C(=CC(=C1Br)Cl)NC=C2OC3C(C(C(C(O3)CO)O)O)O
  • Isomeric SMILES:C1=C2C(=CC(=C1Br)Cl)NC=C2O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O
Technology Process of 5-Bromo-6-chloro-3-indoxyl-beta-D-glucopyranoside

There total 1 articles about 5-Bromo-6-chloro-3-indoxyl-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:
Guidance literature:
1-Acetyl-5-brom-6-chlor-3-indolyl-tetra-O-acetyl-β-D-galactopyranosid i. Me. u. Na-methoxid /5grad;
DOI:10.1021/jm00334a044
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