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4132-28-9,MFCD00066004
Catalog No.:AA0032UC

4132-28-9 | 2,3,4,6-Tetra-o-benzyl-d-glucopyranose

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$6.00   $4.00
- +
25g
98%
in stock  
$16.00   $11.00
- +
100g
98%
in stock  
$22.00   $15.00
- +
500g
98%
in stock  
$105.00   $74.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0032UC
Chemical Name:
2,3,4,6-Tetra-o-benzyl-d-glucopyranose
CAS Number:
4132-28-9
Molecular Formula:
C34H36O6
Molecular Weight:
540.6460
MDL Number:
MFCD00066004
SMILES:
OC1OC(COCc2ccccc2)C(C(C1OCc1ccccc1)OCc1ccccc1)OCc1ccccc1
Properties
Properties
 
BP:
672.4°C at 760 mmHg  
Form:
Solid  
MP:
145-149 °C(lit.)  
Solubility:
Soluble in chloroform  
Storage:
Keep in dry area;-20 ℃;  

Computed Properties
 
Complexity:
665  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
4  
Heavy Atom Count:
40  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
13  
Undefined Atom Stereocenter Count:
1  
XLogP3:
5  

Downstream Synthesis Route

[1]Synlett,1999,p.1420-1422

16001-93-7    4132-28-9    4291-69-4   
((2S,3S,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-ylmethyl)-phosphonicaciddimethylester 

[1]TetrahedronLetters,2001,vol.42,p.5305-5308

16001-93-7    4132-28-9   
((1E,3Z)-(5S,6R)-3,5,7-Tris-benzyloxy-6-hydroxy-hepta-1,3-dienyl)-phosphonicaciddimethylester 

[1]TetrahedronLetters,2001,vol.42,p.5305-5308

[1]Heterocycles,2003,vol.61,p.51-57

5513-40-6    4132-28-9   
4-O-(2,3,4,6-tetra-O-benzyl-α-L-glucopyranosyl)-N-benzyloxycarbonyl-L-tyrosinebenzylester 
 
4-O-(2,3,4,6-tetra-O-benzyl-β-L-glucopyranosyl)-N-benzyloxycarbonyl-L-tyrosinebenzylester 

[1]BioorganicandMedicinalChemistry,2007,vol.15,p.97-103

Literature

Title: Tuning of the prolyl trans/cis-amide rotamer population by use of C-glucosylproline hybrids.

Journal: The Journal of organic chemistry 20070622

Title: Biosynthetic studies on the alpha-glucosidase inhibitor acarbose: the chemical synthesis of isotopically labeled 2-epi-5-epi-valiolone analogs.

Journal: Carbohydrate research 20030926

Title: Potential bile acid metabolites. 24. An efficient synthesis of carboxyl-linked glucosides and their chemical properties.

Journal: Lipids 20020101

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SDS
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Tags:4132-28-9 Molecular Formula|4132-28-9 MDL|4132-28-9 SMILES|4132-28-9 2,3,4,6-Tetra-o-benzyl-d-glucopyranose