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120221-14-9,MFCD00037475
Catalog No.:AA008YJE

120221-14-9 | (2S,3R,4S,5S,6R)-2-(2-Chloro-4-nitrophenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
95%
in stock  
$16.00   $12.00
- +
250mg
95%
in stock  
$23.00   $16.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA008YJE
Chemical Name:
(2S,3R,4S,5S,6R)-2-(2-Chloro-4-nitrophenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
CAS Number:
120221-14-9
Molecular Formula:
C12H14ClNO8
Molecular Weight:
335.6945
MDL Number:
MFCD00037475
SMILES:
OC[C@H]1O[C@@H](Oc2ccc(cc2Cl)N(=O)=O)[C@@H]([C@H]([C@@H]1O)O)O
Properties
Computed Properties
 
Complexity:
394  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
5  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
22  
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:
0.1  

Downstream Synthesis Route
1263-76-9    120221-14-9    145072-72-6   
o-chloro-p-nitrophenyl31-O-maltotriosyl-β-D-glucopyranoside 

[1]CarbohydrateResearch,1993,vol.250,p.57-66

99304-80-0    143206-27-3    120221-14-9   
(2R,3R,4S,5S,6R)-2-{(2R,3S,4R,5R,6R)-6-(2R,3S,4R,5R,6S)-6-(2-Chloro-4-nitro-phenoxy)-4,5-dihydroxy-2-hydroxymethyl-tetrahydro-pyran-3-yloxy-4,5-dihydroxy-2-hydroxymethyl-tetrahydro-pyran-3-yloxy}-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol 

[1]CarbohydrateResearch,2000,vol.329,p.579-585

145072-72-6    143206-27-3    120221-14-9   
(2R,3R,4S,5S,6R)-2-{(2R,3S,4R,5R,6R)-6-(2R,3S,4R,5R,6S)-6-(2-Chloro-4-nitro-phenoxy)-4,5-dihydroxy-2-hydroxymethyl-tetrahydro-pyran-3-yloxy-4,5-dihydroxy-2-hydroxymethyl-tetrahydro-pyran-3-yloxy}-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol 

[1]CarbohydrateResearch,2000,vol.329,p.579-585

[1]JournalofOrganicChemistry,2005,vol.70,p.7217-7226

[1]OrganicLetters,2012,vol.14,p.5086-5089

[2]AngewandteChemie-InternationalEdition,2016,vol.55,p.12338-12342    Angew.Chem.,2016,vol.128,p.12526-12530,5

Literature

Title: Using simple donors to drive the equilibria of glycosyltransferase-catalyzed reactions.

Journal: Nature chemical biology 20111001

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SDS
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Tags:120221-14-9 Molecular Formula|120221-14-9 MDL|120221-14-9 SMILES|120221-14-9 (2S,3R,4S,5S,6R)-2-(2-Chloro-4-nitrophenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
Catalog No.: AA008YJE
120221-14-9,MFCD00037475
120221-14-9 | (2S,3R,4S,5S,6R)-2-(2-Chloro-4-nitrophenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
Pack Size： 100mg
Purity： 95%
in stock
$16.00 $12.00
Pack Size： 250mg
Purity： 95%
in stock
$23.00 $16.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA008YJE
Chemical Name: (2S,3R,4S,5S,6R)-2-(2-Chloro-4-nitrophenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
CAS Number: 120221-14-9
Molecular Formula: C12H14ClNO8
Molecular Weight: 335.6945
MDL Number: MFCD00037475
SMILES: OC[C@H]1O[C@@H](Oc2ccc(cc2Cl)N(=O)=O)[C@@H]([C@H]([C@@H]1O)O)O
Properties
Complexity: 394  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 5  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 22  
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: 0.1  
Downstream Synthesis Route
1263-76-9    120221-14-9    145072-72-6   
o-chloro-p-nitrophenyl31-O-maltotriosyl-β-D-glucopyranoside 

[1]CarbohydrateResearch,1993,vol.250,p.57-66

99304-80-0    143206-27-3    120221-14-9   
(2R,3R,4S,5S,6R)-2-{(2R,3S,4R,5R,6R)-6-(2R,3S,4R,5R,6S)-6-(2-Chloro-4-nitro-phenoxy)-4,5-dihydroxy-2-hydroxymethyl-tetrahydro-pyran-3-yloxy-4,5-dihydroxy-2-hydroxymethyl-tetrahydro-pyran-3-yloxy}-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol 

[1]CarbohydrateResearch,2000,vol.329,p.579-585

145072-72-6    143206-27-3    120221-14-9   
(2R,3R,4S,5S,6R)-2-{(2R,3S,4R,5R,6R)-6-(2R,3S,4R,5R,6S)-6-(2-Chloro-4-nitro-phenoxy)-4,5-dihydroxy-2-hydroxymethyl-tetrahydro-pyran-3-yloxy-4,5-dihydroxy-2-hydroxymethyl-tetrahydro-pyran-3-yloxy}-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol 

[1]CarbohydrateResearch,2000,vol.329,p.579-585

120221-14-9    2280-44-6    619-08-9 

[1]JournalofOrganicChemistry,2005,vol.70,p.7217-7226

572-09-8    120221-14-9 

[1]OrganicLetters,2012,vol.14,p.5086-5089

[2]AngewandteChemie-InternationalEdition,2016,vol.55,p.12338-12342    Angew.Chem.,2016,vol.128,p.12526-12530,5

Literature fold

Title: Using simple donors to drive the equilibria of glycosyltransferase-catalyzed reactions.

Journal: Nature chemical biology20111001

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