CAS 10139-02-3|2-Nitrophenyl 2-acetamido-2-deoxyhexopyranoside
| Common Name | 2-Nitrophenyl 2-acetamido-2-deoxyhexopyranoside | ||
|---|---|---|---|
| CAS Number | 10139-02-3 | Molecular Weight | 342.301 |
| Density | 1.5±0.1 g/cm3 | Boiling Point | 685.2±55.0 °C at 760 mmHg |
| Molecular Formula | C14H18N2O8 | Melting Point | 264ºC |
| MSDS | USA | Flash Point | 368.2±31.5 °C |
Names
| Name | P-NITROPHENYL 2-ACETAMIDO-2-DEOXY-α-D-GLUCOPYRANOSIDE |
|---|---|
| Synonym | More Synonyms |
BiologicalActivity
| Description | 4-Nitrophenyl N-acetyl-α-D-glucosaminide is a 4-nitrophenyl- conjugated substrate for determining the enzymatic specificity[1]. |
|---|---|
| Related Catalog | Research Areas >>OthersSignaling Pathways >>Others >>Others |
| References | [1]. Daniel Garrido, et al. Release and utilization of N-acetyl-D-glucosamine from human milk oligosaccharides by Bifidobacterium longum subsp. Infantis. Anaerobe. 2012 Aug;18(4):430-5. |
Chemical & Physical Properties
| Density | 1.5±0.1 g/cm3 |
|---|---|
| Boiling Point | 685.2±55.0 °C at 760 mmHg |
| Melting Point | 264ºC |
| Molecular Formula | C14H18N2O8 |
| Molecular Weight | 342.301 |
| Flash Point | 368.2±31.5 °C |
| Exact Mass | 342.106323 |
| PSA | 154.07000 |
| LogP | -0.30 |
| Vapour Pressure | 0.0±2.2 mmHg at 25°C |
| Index of Refraction | 1.620 |
| InChIKey | OMRLTNCLYHKQCK-KSTCHIGDSA-N |
| SMILES | CC(=O)NC1C(Oc2ccc([N+](=O)[O-])cc2)OC(CO)C(O)C1O |
| Storage condition | −20°C |
Safety Information
| Safety Phrases | S24/25 |
|---|---|
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
Articles21
More Articles| Syntheses of the 3- and 4-thio analogues of 4-nitrophenyl 2-acetamido-2-deoxy-beta-D-gluco- and galactopyranoside. Carbohydr. Res. 342(15) , 2212-22, (2007) The syntheses of 4-nitrophenyl beta-glycosides of the 3-thio and 4-thio analogues of the two principal 2-acetamido-2-deoxy-hexoses found in living systems, GlcNAc and GalNAc, are described. While synt... | |
| Chitin oligosaccharide synthesis by rhizobia and zebrafish embryos starts by glycosyl transfer to O4 of the reducing-terminal residue. Biochemistry 38(13) , 4045-52, (1999) Lipochitin oligosaccharides are organogenesis-inducing signal molecules produced by rhizobia to establish the formation of nitrogen-fixing root nodules in leguminous plants. Chitin oligosaccharide bio... | |
| Purification and characterization of beta-N-acetylhexosaminidase from Trichoderma harzianum. Agric. Biol. Chem. 55(11) , 2817-23, (1991) beta-N-Acetylhexosaminidase was produced by Trichoderma harzianum cultivated with chitin as the growth substrate. The enzyme was purified 13.2-fold to homogeneity by ultrafiltration and sequential chr... |
Synonyms
| 2-Nitrophenyl 2-acetamido-2-deoxyhexopyranoside |
| Hexopyranoside, 2-nitrophenyl 2-(acetylamino)-2-deoxy- |
| 4-Nitrophenyl N-acetyl-1-thio-|A-D-glucosaminide |
| MFCD00006592 |
| p-Nitrophenyl 2-Acetamido-2-deoxy-Alpha-D-glucopyranoside |
| EINECS 233-392-9 |
| p-nitrophenyllacto-N-biose |
| p-Nitrophenyl 2-acetamido-2-deoxy-1-thio-|A-D-glucopyranoside |
