Iretol

Modify Date: 2024-01-11 00:13:56

Iretol Structure
Iretol structure
Common Name Iretol
CAS Number 487-71-8 Molecular Weight 156.13600
Density 1.436g/cm3 Boiling Point 323.1ºC at 760 mmHg
Molecular Formula C7H8O4 Melting Point N/A
MSDS N/A Flash Point 149.2ºC

 Use of Iretol


Iretol (2,4,6-trihydroxyanisole) is a a degradation product of a glucoside obtained from Iris Jorentina. Iretol is an intermediate in the synthesis of natural isoflavones, such as Tectorigenin, Irigenin and Caviunin[1].

 Names

Name 2-methoxybenzene-1,3,5-triol
Synonym More Synonyms

 Iretol Biological Activity

Description Iretol (2,4,6-trihydroxyanisole) is a a degradation product of a glucoside obtained from Iris Jorentina. Iretol is an intermediate in the synthesis of natural isoflavones, such as Tectorigenin, Irigenin and Caviunin[1].
Related Catalog
References

[1]. Zhu-Ping Xiao, et al. 2,4,6-Trihydroxyanisole. Acta Cryst. (2007). E63, o2941.

 Chemical & Physical Properties

Density 1.436g/cm3
Boiling Point 323.1ºC at 760 mmHg
Molecular Formula C7H8O4
Molecular Weight 156.13600
Flash Point 149.2ºC
Exact Mass 156.04200
PSA 69.92000
LogP 0.81200
Vapour Pressure 0.000141mmHg at 25°C
Index of Refraction 1.627

 Safety Information

HS Code 2909499000

 Synthetic Route

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Iretol Structure

Iretol

CAS#:487-71-8

Literature: Kohner Monatshefte fuer Chemie, 1899 , vol. 20, p. 928

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Iretol Structure

Iretol

CAS#:487-71-8

Literature: Damschroder; Shriner Journal of the American Chemical Society, 1937 , vol. 59, p. 931

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Iretol Structure

Iretol

CAS#:487-71-8

Literature: Shibata Yakugaku Zasshi, 1927 , # 543 p. 61 Chem. Zentralbl., 1927 , vol. 98, # II p. 839

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Iretol Structure

Iretol

CAS#:487-71-8

Detail
Literature: de Laire; Tiemann Chemische Berichte, 1893 , vol. 26, p. 2019

 Customs

HS Code 2909499000
Summary 2909499000. ether-alcohols and their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:5.5%. General tariff:30.0%

 Synonyms

2,4,6-trihydroxyanisole
1,3,5-trihydroxy-2-methoxybenzene
2,4,6-Trihydroxy-1-methoxy-benzol
1.3.5-Trioxy-2-methoxy-benzol
2-Methoxy-phloroglucin
2-METHOXY-BENZENE-1,3,5-TRIOL
2-Methoxy-phloroglucinol