+1 858-523-8231
Login | Register
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
Home Nitro Compounds 3482-57-3
3482-57-3,MFCD00069845
Catalog No.:AA003LTH

3482-57-3 | 4-Nitrophenyl beta-d-cellobioside

Pack Size
Purity
Availability
Price(USD)
Quantity
  
25mg
≥98%
in stock  
$63.00   $44.00
- +
50mg
≥98%
in stock  
$120.00   $84.00
- +
100mg
in stock  
$161.00   $113.00
- +
250mg
in stock  
$212.00   $148.00
- +
500mg
in stock  
$324.00   $227.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003LTH
Chemical Name:
4-Nitrophenyl beta-d-cellobioside
CAS Number:
3482-57-3
Molecular Formula:
C18H25NO13
Molecular Weight:
463.3900
MDL Number:
MFCD00069845
SMILES:
OC[C@H]1O[C@@H](Oc2ccc(cc2)[N+](=O)[O-])[C@@H]([C@H]([C@@H]1O[C@@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)O)O)O)O
Properties
Properties
 
BP:
795.6°C at 760 mmHg  
Form:
Solid  
MP:
249-250°C  
Solubility:
methanol: water (2:3): 50 mg/mL, clear, faintly yellow  
Storage:
2-8℃;  

Computed Properties
 
Complexity:
612  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
10  
Heavy Atom Count:
32  
Hydrogen Bond Acceptor Count:
13  
Hydrogen Bond Donor Count:
7  
Rotatable Bond Count:
6  
XLogP3:
-2.6  

Downstream Synthesis Route

[1]EuropeanJournalofOrganicChemistry,2013,p.2414-2419

[2]JournaloftheAmericanChemicalSociety,1998,vol.120,p.5583-5584

[3]JournaloftheAmericanChemicalSociety,1998,vol.120,p.5583-5584

[4]ProteinScience,2014,vol.23,p.1738-1752

3482-57-3    2106-10-7   
(2S,3R,4S,5S,6R)-2-{(2S,3R,4S,5R,6R)-2-(2R,3S,4R,5R,6S)-4,5-Dihydroxy-2-hydroxymethyl-6-(4-nitro-phenoxy)-tetrahydro-pyran-3-yloxy-3,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-4-yloxy}-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol 
 
C24H35NO18 

[1]EuropeanJournalofOrganicChemistry,2005,p.1977-1983

[2]EuropeanJournalofOrganicChemistry,2005,p.1977-1983

[1]EuropeanJournalofOrganicChemistry,2013,p.2414-2419

7585-39-9    2492-87-7    3482-57-3   
p-nitrophenyl-β-D-glucopyranosyl-(1→6)-O-α-D-glucopyranoside 
 
p-nitrophenyl-β-D-glucopyranosyl-(1→3)-O-α-D-glucopyranoside 

[1]CarbohydrateResearch,2015,vol.404,p.46-54

[1]CarbohydrateResearch,2015,vol.404,p.46-54

Literature

Title: The kinetics of p-nitrophenyl-β-D-cellobioside hydrolysis and transglycosylation by Thermobifida fusca Cel5Acd.

Journal: Carbohydrate research 20101122

Title: Structural changes of cellobiohydrolase I (1,4-beta-D-glucan-cellobiohydrolase I, CBHI) and PNPC (p-nitrophenyl-beta-D-cellobioside) during the binding process.

Journal: Science in China. Series C, Life sciences 20080501

Title: Kinetic characterization of glycosidase activity from disaccharide conjugate to monosaccharide conjugate in Caco-2 cells.

Journal: The Journal of pharmacy and pharmacology 20050501

Title: Biochemical and catalytic properties of an endoxylanase purified from the culture filtrate of Sporotrichum thermophile.

Journal: Carbohydrate research 20030901

Title: A monovalent anion affected multi-functional cellulase EGX from the mollusca, Ampullaria crossean.

Journal: Protein expression and purification 20030901

Title: Purification and some properties of a beta-glucosidase from Trichoderma harzianum type C-4.

Journal: Bioscience, biotechnology, and biochemistry 20010901

Title: Purification and characterization of a cellulase from the ruminal fungus Orpinomyces joyonii cloned in Escherichia coli.

Journal: The international journal of biochemistry & cell biology 20010101

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Related Products of 3482-57-3
1154-94-5

1154-94-5

 102717-16-8

102717-16-8

 100645-45-2

100645-45-2

 14131-42-1

14131-42-1

 147103-31-9

147103-31-9

 1223-07-0

1223-07-0
Building Blocks
More >
Tags:3482-57-3 Molecular Formula|3482-57-3 MDL|3482-57-3 SMILES|3482-57-3 4-Nitrophenyl beta-d-cellobioside