Iretol structure
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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 IretolIretol (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]. |
| Name | 2-methoxybenzene-1,3,5-triol |
|---|---|
| Synonym | More Synonyms |
| 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]. |
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| Related Catalog | |
| References |
[1]. Zhu-Ping Xiao, et al. 2,4,6-Trihydroxyanisole. Acta Cryst. (2007). E63, o2941. |
| 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 |
| InChIKey | ASTPOGDWGNJVEW-UHFFFAOYSA-N |
| SMILES | COc1c(O)cc(O)cc1O |
| HS Code | 2909499000 |
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Iretol CAS#:487-71-8 |
| Literature: Kohner Monatshefte fuer Chemie, 1899 , vol. 20, p. 928 |
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Iretol CAS#:487-71-8 |
| Literature: Damschroder; Shriner Journal of the American Chemical Society, 1937 , vol. 59, p. 931 |
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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 CAS#:487-71-8
Detail
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| Literature: de Laire; Tiemann Chemische Berichte, 1893 , vol. 26, p. 2019 |
| 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% |
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Name: ERK5 transcriptional activity HTS
Source: 24565
Target: N/A
External Id: ERK5 transcriptional activity-HTS
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Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1100
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|
Name: qHTS for Stage-Specific Inhibitors of Vaccinia Orthopoxvirus: mCherry Reporter Primar...
Source: NCGC
Target: 67.9K protein [Vaccinia virus]
External Id: Vaccinia-p2mCherry
|
|
Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1101
|
|
Name: Spectrum HTS for Inhibitors of Aerobactin Synthetase IucA
Source: 23265
Target: IucA Synthetase from hypervirulent Klebsiella pneumoniae hvKP1
External Id: IucA Pilot Assay Spectrum Library
|
|
Name: Inhibition of sodium fluorescein uptake in OATP1B3-transfected CHO cells at an equimo...
Source: ChEMBL
Target: Solute carrier organic anion transporter family member 1B3
External Id: CHEMBL3039491
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|
Name: The chemical genetic matrix (CGM) dataset as reported in Wildenhain et al. (2015) Pre...
Source: 11924
Target: N/A
External Id: CGM data for Cell Systems paper Dec 2015
|
|
Name: qHTS for Stage-Specific Inhibitors of Vaccinia Orthopoxvirus: Venus Reporter Primary ...
Source: NCGC
Target: 67.9K protein [Vaccinia virus]
External Id: Vaccinia-p2Venus
|
|
Name: High Throughput Screening of small molecules that kill Mycobacterium tuberculosis
Source: 15607
Target: N/A
External Id: Cornell_MTB_2017
|
|
Name: qHTS for Inhibitors of binding or entry into cells for Marburg Virus
Source: NCGC
Target: gene 4 small orf - Marburg virus
External Id: VSVM-OFFLINE
|
| 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 |