CAS 3459-18-5|4-Nitrophenyl 2-acetamido-2-deoxyhexopyranoside

Introduction:Basic information about CAS 3459-18-5|4-Nitrophenyl 2-acetamido-2-deoxyhexopyranoside, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name4-Nitrophenyl 2-acetamido-2-deoxyhexopyranoside
CAS Number3459-18-5Molecular Weight342.301
Density1.5±0.1 g/cm3Boiling Point694.7±55.0 °C at 760 mmHg
Molecular FormulaC14H18N2O8Melting Point210 - 212ºC
MSDSChineseUSAFlash Point374.0±31.5 °C

Names

Name4-NITROPHENYL-N-ACETYL-β-D-GLUCOSAMINIDE
SynonymMore Synonyms

BiologicalActivity

Description4-Nitrophenyl-N-acetyl-β-D-glucosaminide, an artificial substrate of N-acetyl-beta-D-hexosaminidase (NAGase), can be used in rapid and accurate rate assay for N-acetyl-beta-D-hexosaminidase[1].
Related CatalogResearch Areas >>Others
References

[1]. Shibata H, et, al. Rate assay of N-acetyl-beta-D-hexosaminidase with 4-nitrophenyl N-acetyl-beta-D-glucosaminide as an artificial substrate. Clin Chim Acta. 1996 Jul 15;251(1):53-64.  

Chemical & Physical Properties

Density1.5±0.1 g/cm3
Boiling Point694.7±55.0 °C at 760 mmHg
Melting Point210 - 212ºC
Molecular FormulaC14H18N2O8
Molecular Weight342.301
Flash Point374.0±31.5 °C
Exact Mass342.106323
PSA154.07000
LogP0.00
Vapour Pressure0.0±2.3 mmHg at 25°C
Index of Refraction1.620
InChIKeyOMRLTNCLYHKQCK-DHGKCCLASA-N
SMILESCC(=O)NC1C(Oc2ccc([N+](=O)[O-])cc2)OC(CO)C(O)C1O
Storage condition−20°C
Water SolubilityH2O: 5 mg/mL, clear, colorless to very faintly yellow

Safety Information

Personal Protective EquipmentEyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard CodesXi: Irritant;
Safety PhrasesS22-S24/25
RIDADRNONH for all modes of transport
WGK Germany3

Articles22

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

4-nitrophenyl-N-acetyl-Beta-D-glucosaminide
EINECS 222-398-7
4-Nitrophenyl 2-acetamido-2-deoxyhexopyranoside
4-Nitrophenyl 2-AcetaMido-2-deoxy-β-D-glucopyranoside
4-Nitrophenyl-2-acetamido-2-deoxy-beta-D-glucopyranoside
Hexopyranoside, 4-nitrophenyl 2-(acetylamino)-2-deoxy-
4-N-pyrrolomethylbenzoic acid
4-Nitrophenyl N-Acetyl-β-D-glucosaminide
MFCD00063696
4-Pyrrol-1-ylmethyl-benzoic acid
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