| Identification | Back Directory | [Name]
P-NITROPHENYL 6-DEOXY-ALPHA-L-MANNOPYRANOSIDE | [CAS]
18918-31-5 | [Synonyms]
-L-Rhamnopyranoside
p-nitrophenyl α-L-Rhap
4-nitrophenylrhamnoside
4-NITROPHENYL-A-L-RHAMNOSIDE
P-NITROPHENYL-ALPHA-RHAMNOSIDE
p-Nitrophenyl alpha-L-rhamnoside
4-NITROPHENYL-ALPHA-L-RHAMNOSIDE
4-Nitrophenyl α-L-rhamnopyranosid
4-Nitrophenyla-L-rhamnopyranoside
3-Nitrophenyl ?L-rhamnopyranoside
3-Nitrophenyl a-L-rhaMnopyranoside
P-nitrophenyl A-L-rhamnopyranoside
4-nitrophenyl α-l-rhamnopyranoside
para-Nitrophenyl-alpha-L-rhamnoside
3-Nitrophenyl alpha-L-rhamnopyranoside
4-NITROPHENYL-ALPHA-L-RHAMNOPYRANOSIDE
P-NITROPHENYL ALPHA-L-RHAMNOPYRANOSIDE
4-Nitrophenyl α-L-rhamnopyranoside ,98%
4-Nitrophenyl 6-deoxy-α-L-mannopyranoside
p-nitrophenyl 6-deoxy-α-l-mannopyranoside
a-L-Mannopyranoside, 4-nitrophenyl6-deoxy-
α-L-Mannopyranoside, 4-nitrophenyl 6-deoxy-
P-NITROPHENYL 6-DEOXY-ALPHA-L-MANNOPYRANOSIDE
P-NITROPHENYL 6-DEOXY-ALPHA-L-MANNOPYRANOSIDE USP/EP/BP
(2S,3R,4R,5R,6S)-2-methyl-6-(4-nitrophenoxy)tetrahydro-2H-pyran-3,4,5-triol | [EINECS(EC#)]
1592732-453-0 | [Molecular Formula]
C12H15NO7 | [MDL Number]
MFCD00069788 | [MOL File]
18918-31-5.mol | [Molecular Weight]
285.25 |
| Chemical Properties | Back Directory | [Melting point ]
179°C | [Boiling point ]
515.4±50.0 °C(Predicted) | [density ]
1.503±0.06 g/cm3(Predicted) | [storage temp. ]
−20°C
| [solubility ]
DMF: 20 mg/ml; DMSO: 15 mg/ml; Ethanol: 0.25 mg/ml; PBS (pH 7.2): 2 mg/ml | [form ]
powder
| [pka]
12.68±0.70(Predicted) | [color ]
Off-white to light yellow | [InChI]
InChI=1/C12H15NO7/c1-6-9(14)10(15)11(16)12(19-6)20-8-4-2-7(3-5-8)13(17)18/h2-6,9-12,14-16H,1H3/t6-,9-,10+,11+,12-/s3 | [InChIKey]
YILIDCGSXCGACV-KOILSSBMNA-N | [SMILES]
[C@H]1(O[C@H]([C@H](O)[C@@H](O)[C@H]1O)C)OC1=CC=C([N+]([O-])=O)C=C1 |&1:0,2,3,5,7,r| | [LogP]
1.170 (est) |
| Hazard Information | Back Directory | [Uses]
4-Nitrophenyl α-L-Rhamnopyranoside is a chromogenic substrate for naringinase. | [Biochem/physiol Actions]
4-Nitrophenyl α-L-rhamnopyranoside is a substrate for determining α-L-rhamnosidase activity. The hydrolysis of 4-Nitrophenyl α-L-rhamnopyranoside by the enzyme yields 4-nitrophenol, measured at 405 nm spectrophotometrically. |
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