Home Nitro Compounds 14948-96-0
14948-96-0,MFCD00067360
Catalog No.:AA001LOE

14948-96-0 | 4-Nitrophenyl 2-acetamido-2-deoxy-beta-d-galactopyranoside

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25mg
95%
in stock  
$65.00   $45.00
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50mg
95%
in stock  
$110.00   $77.00
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100mg
95%
in stock  
$174.00   $122.00
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250mg
95%
in stock  
$192.00   $134.00
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1g
> 98% (HPLC)
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$502.00   $352.00
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2.5g
> 98% (HPLC)
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$958.00   $671.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA001LOE
Chemical Name:
4-Nitrophenyl 2-acetamido-2-deoxy-beta-d-galactopyranoside
CAS Number:
14948-96-0
Molecular Formula:
C14H18N2O8
Molecular Weight:
342.3013
MDL Number:
MFCD00067360
SMILES:
OC[C@H]1O[C@@H](Oc2ccc(cc2)[N+](=O)[O-])[C@@H]([C@H]([C@H]1O)O)NC(=O)C
Properties
Computed Properties
 
Complexity:
449  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
5  
Heavy Atom Count:
24  
Hydrogen Bond Acceptor Count:
8  
Hydrogen Bond Donor Count:
4  
Rotatable Bond Count:
4  
XLogP3:
-0.4  

Downstream Synthesis Route

[1]Chen,Hong-Ming;Withers,StephenG.[CarbohydrateResearch,2007,vol.342,#15,p.2212-2222]

[2]Heyworthetal.[JournaloftheChemicalSociety,1959,p.4121]Watkins[BiochemicalJournal,1959,vol.71,p.261,262]

[1]Crout,DavidH.;Singh,Suddham;Swoboda,BenE.P.G.;Critchley,Peter;Gibson,WalterT.[JournaloftheChemicalSociety.Chemicalcommunications,1992,#9,p.704-705]

[1]Crout,DavidH.;Singh,Suddham;Swoboda,BenE.P.G.;Critchley,Peter;Gibson,WalterT.[JournaloftheChemicalSociety.Chemicalcommunications,1992,#9,p.704-705]

[2]Crout,DHG;MacManus,DA;Ricca,J-M;Singh,S;Critchley,P;Gibson,WT[IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1993,vol.32,#1,p.195-201]

Lactose 
  14948-96-0   
p-nitrophenyl2-acetamido-2-deoxy-4-O-β-D-galactopyranosyl-β-D-galactoside 

[1]Usui;Kubota;Ohi[CarbohydrateResearch,1993,vol.244,#2,p.315-323]

[1]Kyosaka;Yamashiro;Tanaka[Chemicalandpharmaceuticalbulletin,1980,vol.28,#9,p.2658-2664]

[2]Farlane,ErnestF.Mc;Farlane,DallasR.Mc;Kennedy,IvanR.[Phytochemistry,1984,vol.23,#11,p.2431-2434]

[3]Senba,Mio;Kashige,Nobuhiro;Miake,Fumio;Watanabe,Kenji[Bioscience,BiotechnologyandBiochemistry,1998,vol.62,#2,p.404-406]

[4]Bayón;Moracci;Hernáiz[RSCAdvances,2015,vol.5,#68,p.55313-55320]

[5]Roth;Petricevic;John;Goddard-Borger;Davies;Williams[ChemicalCommunications,2016,vol.52,#74,p.11096-11099]

Literature

Title: Characterization of glycosyl hydrolase family 3 beta-N-acetylglucosaminidases from Thermotoga maritima and Thermotoga neapolitana.

Journal: Journal of bioscience and bioengineering 20091201

Title: Inactivation kinetics of beta-N-acetyl-D-glucosaminidase from green crab (Scylla serrata) in dioxane solution.

Journal: Journal of biomolecular structure & dynamics 20090201

Title: Syntheses of the 3- and 4-thio analogues of 4-nitrophenyl 2-acetamido-2-deoxy-beta-D-gluco- and galactopyranoside.

Journal: Carbohydrate research 20071105

Title: Purification and characterization of beta-N-acetylhexosaminidase from rice seeds.

Journal: Journal of biochemistry and molecular biology 20020531

Title: Amino acid sequence and carbohydrate-binding analysis of the N-acetyl-D-galactosamine-specific C-type lectin, CEL-I, from the Holothuroidea, Cucumaria echinata.

Journal: Bioscience, biotechnology, and biochemistry 20020101

Title: Glycosidase activity in the post-ecdysial cuticle of the blue crab, Callinectes sapidus.

Journal: Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology 20010401

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SDS
Tags:14948-96-0 Molecular Formula|14948-96-0 MDL|14948-96-0 SMILES|14948-96-0 4-Nitrophenyl 2-acetamido-2-deoxy-beta-d-galactopyranoside