1,2,3,4-Tetra-o-acetyl-ß-D-glucopyranuronate

Names

[ Name ]:
1,2,3,4-Tetra-o-acetyl-ß-D-glucopyranuronate

[Synonym ]:
T6OTJ BVO1 COV1 DOV1 EOV1 FOV1 &&β-D-Gluco Form
1,2,3,4-Tetra-o-acetyl-ß-D-glucopyranuronate
Methyl 3,4,5,6-tetra(acetyloxy)tetrahydro-2H-pyran-2-carboxylate
Methyl 1,2,3,4-tetra-O-acetyl-β-D-glucopyranuronate
Methyl O-tetraacetyl-β-D-glucopyranuronate
Methyl 1,2,3,4-Tetra-O-acetyl-β-D-glucuronate
EINECS 230-880-3
β-D-Glucopyranuronic acid, methyl ester, 1,2,3,4-tetraacetate
β-D-Glucopyranuronic acid, methyl ester, tetraacetate
MFCD00069834

Biological Activity

[Description]:

Methyl tetra-O-acetyl-β-D-glucopyranuronate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
412.3±45.0 °C at 760 mmHg

[ Melting Point ]:
179 °C

[ Molecular Formula ]:
C₁₅H₂₀O₁₁

[ Molecular Weight ]:
376.31

[ Flash Point ]:
178.4±28.8 °C

[ Exact Mass ]:
376.100555

[ PSA ]:
140.73000

[ LogP ]:
1.88

[ Vapour Pressure ]:
0.0±1.0 mmHg at 25°C

[ Index of Refraction ]:
1.482

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Articles

Design and synthesis of water-soluble glucuronide derivatives of camptothecin for cancer prodrug monotherapy and antibody-directed enzyme prodrug therapy (ADEPT).

J. Med. Chem. 42 , 3623-8, (1999)

Glucuronide prodrugs of 9-aminocamptothecin were synthesized. Prodrug 4, in which 9-aminocamptothecin was connected to glucuronic acid by an aromatic spacer via a carbamate linkage, was stable in both...

Synthesis and role of glycosylthio heterocycles in carbohydrate chemistry Ashry, E., et al.

Tetrahedron 62 , 2943-98, (2006)

Related Compounds

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