ChemicalBook--->CAS DataBase List--->1223-07-0

1223-07-0

1223-07-0 Structure

1223-07-0 Structure
IdentificationBack Directory
[Name]

P-NITROPHENYL ALPHA-L-ARABINOPYRANOSIDE
[CAS]

1223-07-0
[Synonyms]

(2S,3R,4S,5S)
-2-(4-Nitrophenoxy)
4-Nitrophenyla-L-arabinopyranoside
P-nitrophenyl-A-L-arabinopyranoside
α-L-Arabinopyranoside, 4-nitrophenyl
P-NITROPHENYL ALPHA-L-ARABINOPYRANOSIDE
4-NITROPHENYL-ALPHA-L-ARABINOPYRANOSIDE
4-Nitrophenyl α-L-arabinopyranoside ,98%
4-nitrophenyl-alpha-laevo-arabinopyranoside
P-NITROPHENYL ALPHA-L-ARABINOPYRANOSIDE USP/EP/BP
(2S,3R,4S,5S)-2-(4-Nitrophenoxy)tetrahydropyran-3,4,5-triol
(2S,3R,4S,5S)-2-(4-nitrophenoxy)tetrahydro-2H-pyran-3,4,5-triol
4-Nitrophenyl alpha-L-arabinopyranoside arabinosidase substrate
[EINECS(EC#)]

1592732-453-0
[Molecular Formula]

C11H13NO7
[MDL Number]

MFCD00151486
[MOL File]

1223-07-0.mol
[Molecular Weight]

271.22
Chemical PropertiesBack Directory
[Melting point ]

205°C
[Boiling point ]

523.2±50.0 °C(Predicted)
[density ]

1.597±0.06 g/cm3(Predicted)
[storage temp. ]

−20°C
[solubility ]

ethanol: water (1:1): 19.60-20.40mg/mL
[form ]

powder
[pka]

12.67±0.70(Predicted)
[InChI]

InChI=1/C11H13NO7/c13-8-5-18-11(10(15)9(8)14)19-7-3-1-6(2-4-7)12(16)17/h1-4,8-11,13-15H,5H2/t8-,9-,10+,11-/s3
[InChIKey]

MLJYKRYCCUGBBV-COCZPBFRNA-N
[SMILES]

[C@H]1(OC[C@H](O)[C@H](O)[C@H]1O)OC1=CC=C([N+]([O-])=O)C=C1 |&1:0,3,5,7,r|
[LogP]

0.680 (est)
Safety DataBack Directory
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

29400090
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

White to off-white crystalline powder
[Uses]

4-Nitrophenyl α-L-arabinopyranoside may be used: as a 4-nitrophenyl-glycoside substrate to study the substrate activities of TlAbf51 by determining the arabinofuranosidase (Abf) activity in standard conditions. It may also be used to determine the activity of α-L-arabinofuranosidase spectrophotometrically.
[Definition]

ChEBI: 4-nitrophenyl alpha-L-arabinoside is an alpha-L-arabinopyranoside having a 4-nitrophenyl substituent at the anomeric position It has a role as a chromogenic compound. It is an alpha-L-arabinopyranoside and a C-nitro compound. It is functionally related to a 4-nitrophenol.
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