| Identification | Back Directory | [Name]
5-BROMO-4-CHLORO-3-INDOLYL ALPHA-D-MANNOPYRANOSIDE | [CAS]
125229-64-3 | [Synonyms]
X-MAN
X-ALPHA-D-MAN
X-A-D-MANNOSIDE
X-ALPHA-MANNOSIDE
X-ALPHA-D-MANNOSIDE
RARECHEM AH BS 0013
5-Bromo-4-chloro-3-indolyl α-D-mannopyranoside
5-bromo-4-chloro-3-indolyl α-d-mannopyranoside
5-bromo-4-chloro-3-indolyl A-D-*mannopyranoside
5-BROMO-4-CHLORO-3-INDOXYL-ALPHA-D-MANNOPYRANOSIDE
5-BROMO-4-CHLORO-3-INDOLYL ALPHA-D-MANNOPYRANOSIDE
a-D-Mannopyranoside, 5-bromo-4-chloro-1H-indol-3-yl
α-D-Mannopyranoside, 5-bromo-4-chloro-1H-indol-3-yl
alpha-D-Mannopyranoside 5-bromo-4-chloro-1H-indol-3-yl
5-BROMO-4-CHLORO-3-INDOLYL ALPHA-D-MANNOPYRANOSIDE USP/EP/BP
(2R,3S,4S,5S,6R)-2-((5-Bromo-4-chloro-1H-indol-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol | [EINECS(EC#)]
803-025-2 | [Molecular Formula]
C14H15BrClNO6 | [MDL Number]
MFCD00078951 | [MOL File]
125229-64-3.mol | [Molecular Weight]
408.63 |
| Chemical Properties | Back Directory | [Boiling point ]
674℃ | [density ]
1.882 | [Fp ]
361℃ | [storage temp. ]
Sealed in dry,Store in freezer, under -20°C | [solubility ]
DMF: 20 mg/mL, clear, colorless to light yellow | [form ]
powder | [InChI]
1S/C14H15BrClNO6/c15-5-1-2-6-9(10(5)16)7(3-17-6)22-14-13(21)12(20)11(19)8(4-18)23-14/h1-3,8,11-14,17-21H,4H2/t8-,11-,12+,13+,14+/m1/s1 | [InChIKey]
OPIFSICVWOWJMJ-HAAGFXOZSA-N | [SMILES]
OC[C@H]1O[C@H](Oc2c[nH]c3ccc(Br)c(Cl)c23)[C@@H](O)[C@@H](O)[C@@H]1O |
| Hazard Information | Back Directory | [Chemical Properties]
White solid | [Uses]
5-Bromo-4-chloro-3-indolyl-α-D-mannopyranoside, 93% is a cationic surfactant commonly used in micelle experiments. | [Definition]
ChEBI: 5-bromo-4-chloro-3-indolyl alpha-D-mannoside is an indolyl carbohydrate that is the alpha-D-mannoside of indoxyl in which the indole moiety is substituted at positions 4 and 5 by chlorine and bromine, respectively It has a role as a chromogenic compound. It is an organobromine compound, an organochlorine compound, an indolyl carbohydrate, a D-aldohexose derivative and an alpha-D-mannoside. It is functionally related to an indoxyl. |
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