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18918-31-5

18918-31-5 Structure

18918-31-5 Structure
IdentificationBack 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 PropertiesBack 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)
Safety DataBack Directory
[WGK Germany ]

3
[HS Code ]

29400090
[Storage Class]

11 - Combustible Solids
Hazard InformationBack 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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