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| | P-NITROPHENYL ALPHA-L-ARABINOPYRANOSIDE Basic information |
| Product Name: | P-NITROPHENYL ALPHA-L-ARABINOPYRANOSIDE | | Synonyms: | P-NITROPHENYL ALPHA-L-ARABINOPYRANOSIDE;P-nitrophenyl-A-L-arabinopyranoside;4-Nitrophenyla-L-arabinopyranoside;(2S,3R,4S,5S)-2-(4-Nitrophenoxy)tetrahydropyran-3,4,5-triol;(2S,3R,4S,5S);-2-(4-Nitrophenoxy);4-NITROPHENYL-ALPHA-L-ARABINOPYRANOSIDE;(2S,3R,4S,5S)-2-(4-nitrophenoxy)tetrahydro-2H-pyran-3,4,5-triol | | CAS: | 1223-07-0 | | MF: | C11H13NO7 | | MW: | 271.22 | | EINECS: | 1592732-453-0 | | Product Categories: | Activity;Arabinoside;Chromogenic;ChromogenicSubstrates;Enzyme Substrates | | Mol File: | 1223-07-0.mol |  |
| | P-NITROPHENYL ALPHA-L-ARABINOPYRANOSIDE Chemical Properties |
| 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) |
| WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29400090 | | Storage Class | 11 - Combustible Solids |
| | P-NITROPHENYL ALPHA-L-ARABINOPYRANOSIDE Usage And Synthesis |
| 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. |
| | P-NITROPHENYL ALPHA-L-ARABINOPYRANOSIDE Preparation Products And Raw materials |
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