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35599-02-1,MFCD00067650
Catalog No.:AA00C0MI

35599-02-1 | 4-Nitrophenyl-beta-d-mannopyranoside

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5mg
≥97%
in stock  
$274.00   $192.00
- +
25mg
≥97%
in stock  
$824.00   $577.00
- +
100mg
≥97%
in stock  
$2,204.00   $1,543.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00C0MI
Chemical Name:
4-Nitrophenyl-beta-d-mannopyranoside
CAS Number:
35599-02-1
Molecular Formula:
C12H15NO8
Molecular Weight:
301.2494
MDL Number:
MFCD00067650
SMILES:
OCC1OC(Oc2ccc(cc2)[N+](=O)[O-])C(C(C1O)O)O C12H15NO8
Properties
Computed Properties
 
Complexity:
354  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
5  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
21  
Hydrogen Bond Acceptor Count:
8  
Hydrogen Bond Donor Count:
4  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-0.4  

Downstream Synthesis Route
35599-02-1    2106-10-7   
C30H45NO23 
 
4-nitrophenylβ-D-glucopyranosyl-(1→4)-β-D-mannopyranoside 
 
(2S,3R,4S,5S,6R)-2-{(2R,3S,4R,5R,6S)-6-(2R,3S,4R,5S,6S)-4,5-Dihydroxy-2-hydroxymethyl-6-(4-nitro-phenoxy)-tetrahydro-pyran-3-yloxy-4,5-dihydroxy-2-hydroxymethyl-tetrahydro-pyran-3-yloxy}-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol 

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

35599-02-1    2106-10-7   
4-nitrophenylβ-D-glucopyranosyl-(1->3)-β-D-mannopyranoside 

[1]CarbohydrateResearch,2006,vol.341,p.2055-2065

1226-39-7    35599-02-1    2106-10-7    2001-96-9    2492-87-7    3150-24-1   
4-nitrophenylβ-D-glucopyranosyl-(1->3)-β-D-fucopyranoside 
 
4-nitrophenylβ-D-glucopyranosyl-(1->3)-β-D-galactopyranoside 
 
C23H33NO17 
 
4-nitrophenylβ-D-glucopyranosyl-(1->4)-β-D-xylopyranoside 
  26255-70-9   
4-nitrophenylβ-D-glucopyranosyl-(1->3)-β-D-xylopyranoside 
 
4-nitrophenylβ-D-glucopyranosyl-(1→4)-β-D-mannopyranoside 
  2713-54-4 

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

35599-02-1    2106-10-7    1433713-08-6   
4-nitrophenylβ-D-glucopyranosyl-(1→4)-β-D-mannopyranoside 

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

Literature

Title: Expression and characterization of an extremely thermostable β-glycosidase (mannosidase) from the hyperthermophilic archaeon Pyrococcus furiosus DSM3638.

Journal: New biotechnology 20111001

Title: [A procedure for determination of acid mannosidase activities in biological fluids].

Journal: Klinicheskaia laboratornaia diagnostika 20090301

Title: Sensitive and rapid electrochemical bioassay of glycosidase activity.

Journal: The Analyst 20060801

Title: Purification and characterization of a beta-D-mannosidase from the marine anaspidean Aplysia fasciata.

Journal: Journal of biotechnology 20050922

Title: Synthesis of beta-mannosides using the transglycosylation activity of endo-beta-mannosidase from Lilium longiflorum.

Journal: The FEBS journal 20050401

Quotation Request
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SDS
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Tags:35599-02-1 Molecular Formula|35599-02-1 MDL|35599-02-1 SMILES|35599-02-1 4-Nitrophenyl-beta-d-mannopyranoside
Catalog No.: AA00C0MI
35599-02-1,MFCD00067650
35599-02-1 | 4-Nitrophenyl-beta-d-mannopyranoside
Pack Size： 5mg
Purity： ≥97%
in stock
$274.00 $192.00
Pack Size： 25mg
Purity： ≥97%
in stock
$824.00 $577.00
Pack Size： 100mg
Purity： ≥97%
in stock
$2,204.00 $1,543.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00C0MI
Chemical Name: 4-Nitrophenyl-beta-d-mannopyranoside
CAS Number: 35599-02-1
Molecular Formula: C12H15NO8
Molecular Weight: 301.2494
MDL Number: MFCD00067650
SMILES: OCC1OC(Oc2ccc(cc2)[N+](=O)[O-])C(C(C1O)O)O C12H15NO8
Properties
Complexity: 354  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 5  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 21  
Hydrogen Bond Acceptor Count: 8  
Hydrogen Bond Donor Count: 4  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -0.4  
Downstream Synthesis Route
35599-02-1    2106-10-7   
C30H45NO23 
 
4-nitrophenylβ-D-glucopyranosyl-(1→4)-β-D-mannopyranoside 
 
(2S,3R,4S,5S,6R)-2-{(2R,3S,4R,5R,6S)-6-(2R,3S,4R,5S,6S)-4,5-Dihydroxy-2-hydroxymethyl-6-(4-nitro-phenoxy)-tetrahydro-pyran-3-yloxy-4,5-dihydroxy-2-hydroxymethyl-tetrahydro-pyran-3-yloxy}-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol 

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

35599-02-1    2106-10-7   
4-nitrophenylβ-D-glucopyranosyl-(1->3)-β-D-mannopyranoside 

[1]CarbohydrateResearch,2006,vol.341,p.2055-2065

1226-39-7    35599-02-1    2106-10-7    2001-96-9    2492-87-7    3150-24-1   
4-nitrophenylβ-D-glucopyranosyl-(1->3)-β-D-fucopyranoside 
 
4-nitrophenylβ-D-glucopyranosyl-(1->3)-β-D-galactopyranoside 
 
C23H33NO17 
 
4-nitrophenylβ-D-glucopyranosyl-(1->4)-β-D-xylopyranoside 
  26255-70-9   
4-nitrophenylβ-D-glucopyranosyl-(1->3)-β-D-xylopyranoside 
 
4-nitrophenylβ-D-glucopyranosyl-(1→4)-β-D-mannopyranoside 
  2713-54-4 

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

35599-02-1    2106-10-7    1433713-08-6   
4-nitrophenylβ-D-glucopyranosyl-(1→4)-β-D-mannopyranoside 

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

Literature fold

Title: Expression and characterization of an extremely thermostable β-glycosidase (mannosidase) from the hyperthermophilic archaeon Pyrococcus furiosus DSM3638.

Journal: New biotechnology20111001

Title: [A procedure for determination of acid mannosidase activities in biological fluids].

Journal: Klinicheskaia laboratornaia diagnostika20090301

Title: Sensitive and rapid electrochemical bioassay of glycosidase activity.

Journal: The Analyst20060801

Title: Purification and characterization of a beta-D-mannosidase from the marine anaspidean Aplysia fasciata.

Journal: Journal of biotechnology20050922

Title: Synthesis of beta-mannosides using the transglycosylation activity of endo-beta-mannosidase from Lilium longiflorum.

Journal: The FEBS journal20050401

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