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41514-64-1

41514-64-1 structure
41514-64-1 structure
  • Name: 3,4,5-trimethoxyphenyl β-glucopyranoside
  • Chemical Name: 3,4,5-Trimethoxyphenyl β-D-glucopyranoside
  • CAS Number: 41514-64-1
  • Molecular Formula: C15H22O9
  • Molecular Weight: 346.330
  • Catalog: Natural product Phenols
  • Create Date: 2016-07-27 15:39:43
  • Modify Date: 2024-01-04 16:18:03
  • Koaburaside monomethyl ether is a phenolic glycoside that can be isolated from Averrhoa carambola L.[1].

Name 3,4,5-Trimethoxyphenyl β-D-glucopyranoside
Synonyms Benzyl alcohol,3,4,5-trimethoxy
3,4,5-trimethoxy-benzenemethanol
3,4,5-Trimethoxyphenyl Beta-D-glucopyranoside
Benzenemethanol,3,4,5-trimethoxy
3,4,5-trimethoxybenzyl alcohol
3,4,5-Trimethoxyphenyl β-D-glucopyranoside
β-D-Glucopyranoside, 3,4,5-trimethoxyphenyl
koaburaside monomethyl ether
3,4,5-trimethoxyphenyl β-glucopyranoside
Description Koaburaside monomethyl ether is a phenolic glycoside that can be isolated from Averrhoa carambola L.[1].
Related Catalog
References

[1]. Wen Q, et al. Phenolic and lignan glycosides from the butanol extract of Averrhoa carambola L. root. Molecules. 2012 Oct 19;17(10):12330-40.  

Density 1.4±0.1 g/cm3
Boiling Point 558.6±50.0 °C at 760 mmHg
Molecular Formula C15H22O9
Molecular Weight 346.330
Flash Point 291.6±30.1 °C
Exact Mass 346.126373
PSA 127.07000
LogP -0.75
Vapour Pressure 0.0±1.6 mmHg at 25°C
Index of Refraction 1.574
Hazard Codes Xi

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41514-64-1 structure

41514-64-1

Literature: Verotta, Luisella; Dell'Agli, Mario; Giolitot, Andrea; Guerrini, Marco; Cabalion, Pierre; Bosisio, Enrica Journal of Natural Products, 2001 , vol. 64, # 5 p. 603 - 607

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41514-64-1 structure

41514-64-1

Literature: Verotta, Luisella; Dell'Agli, Mario; Giolitot, Andrea; Guerrini, Marco; Cabalion, Pierre; Bosisio, Enrica Journal of Natural Products, 2001 , vol. 64, # 5 p. 603 - 607

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41514-64-1 structure

41514-64-1

Literature: Verotta, Luisella; Dell'Agli, Mario; Giolitot, Andrea; Guerrini, Marco; Cabalion, Pierre; Bosisio, Enrica Journal of Natural Products, 2001 , vol. 64, # 5 p. 603 - 607
Precursor  3

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