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| | 5-BROMO-4-CHLORO-3-INDOLYL-ALPHA-D-GLUCOPYRANOSIDE Basic information |
| Product Name: | 5-BROMO-4-CHLORO-3-INDOLYL-ALPHA-D-GLUCOPYRANOSIDE | | Synonyms: | 5-BROMO-4-CHLORO-3-INDOLYL-ALPHA-D-GLUCOPYRANOSIDE5-BROMO-4-CHLORO-3-INDOLYL-ALPHA-D-GLUCOPYRANOSIDE;(2R,3R,4S,5S,6R)-2-[(5-Bromo-4-chloro-1H-indol-3-yl)oxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol;5-BROMO-4-CHLORO-3-INDOLYL-ALPHA-D-GLUCOPYRANOSIDE;5-BROMO-4-CHLORO-3-INDOLYL-ALPHA-D-GLUCOSIDE;5-BROMO-4-CHLORO-3-INDOXYL-ALPHA-D-GLUCOPYRANOSIDE;X-ALPHA-D-GLC;X-ALPHA-D-GLUCOSIDE;X-ALPHA-GLU | | CAS: | 108789-36-2 | | MF: | C14H15BrClNO6 | | MW: | 408.63 | | EINECS: | 1533716-785-6 | | Product Categories: | substrate | | Mol File: | 108789-36-2.mol |  |
| | 5-BROMO-4-CHLORO-3-INDOLYL-ALPHA-D-GLUCOPYRANOSIDE Chemical Properties |
| Boiling point | 674℃ | | density | 1.882 | | refractive index | 1.6110 (estimate) | | Fp | 361℃ | | storage temp. | -20°C | | form | powder | | pka | 12.74±0.70(Predicted) | | color | White | | optical activity | [α]/D 105.0±5.0°, c = 1 in DMF/H2O 1:1 |
| WGK Germany | 3 | | HS Code | 29400090 |
| | 5-BROMO-4-CHLORO-3-INDOLYL-ALPHA-D-GLUCOPYRANOSIDE Usage And Synthesis |
| Chemical Properties | white to off-white fine crystalline powder | | Uses | suitable as substrate for α-glucosidase; substrate used in the Druggan-Forsythe-Iversen medium (DFI agar) for the selective detection of Enterobacter sakazakii in infant milk | | Definition | ChEBI: 5-bromo-4-chloro-3-indolyl alpha-D-glucoside is an indolyl carbohydrate that is the alpha-D-glucoside of indoxyl in which the indole moiety is substituted at positions 4 and 5 by chlorine and bromine, respectively. It is an organobromine compound, an organochlorine compound, an indolyl carbohydrate, a D-aldohexose derivative and an alpha-D-glucoside. It is functionally related to an indoxyl. | | General Description | 5-Bromo-4-chloro-3-indolyl α-D-glucopyranoside, X-Gluc, is a indigogenic substrate for β- glucuronidase enzyme (GUS). It aids screening of transgenic plants based on GUS activity. GUS deesterifies X-Gluc into indoxyl derivative which upon oxidative polymerization results in the generation of blue indigotin dye. |
| | 5-BROMO-4-CHLORO-3-INDOLYL-ALPHA-D-GLUCOPYRANOSIDE Preparation Products And Raw materials |
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