CAS Number31524-62-6
Synonyms4',7-dihydroxy-8-prenylflavanone; (+-)-6-chloro-7; SK&6-Chlor-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepin; (2S)-7-Hydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-2,3-dihydro-4H-chromen-4-one; 6-chloro-1-phenyl-2,3,4,5-tetrahydro-1h-3-benzazepine-7,8-diol; 6-Chloro-2,3,4,5-tetrahydro-1-phenyl-1H-3-benzazepine-7,8-diol; 8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine; 1H-3-Benzazepine-7,8-diol,6-chloro-2,3,4,5-tetrahydro-1-phenyl; 8-prenylliquiritigenin; 8-dimethylallylliquiritigenin; 6-chloro-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine
Molecular FormulaC20H20O4
Molecular Weight324.370
Density1.2±0.1 g/cm3
Boiling Point558.3±50.0 °C at 760 mmHg
Melting Point187-188℃
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 31524-62-6 |
| Catalog No. | 2A-9065844 |
| Chinese Name | 异补骨脂黄酮 |
| Synonyms | 4',7-dihydroxy-8-prenylflavanone; (+-)-6-chloro-7; SK&6-Chlor-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepin; (2S)-7-Hydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-2,3-dihydro-4H-chromen-4-one; 6-chloro-1-phenyl-2,3,4,5-tetrahydro-1h-3-benzazepine-7,8-diol; 6-Chloro-2,3,4,5-tetrahydro-1-phenyl-1H-3-benzazepine-7,8-diol; 8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine; 1H-3-Benzazepine-7,8-diol,6-chloro-2,3,4,5-tetrahydro-1-phenyl; 8-prenylliquiritigenin; 8-dimethylallylliquiritigenin; 6-chloro-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine |
| Molecular Formula | C20H20O4 |
| Molecular Weight | 324.370 |
| Density | 1.2±0.1 g/cm3 |
| Boiling Point | 558.3±50.0 °C at 760 mmHg |
| Melting Point | 187-188℃ |
| Storage Condition | 2-8C |
| Application | Isobavachin is an antioxidant that can be isolated from Psoralea morisiana. It has a prenyl group at position 8 of the A ring, which can promote the differentiation of neurons and the potential role o |
| HTC | 2932999099 |
| SMILES | CC(C)=CCc1c(O)ccc2c1OC(c1ccc(O)cc1)CC2=O |
| InChI | InChI=1S/C20H20O4/c1-12(2)3-8-15-17(22)10-9-16-18(23)11-19(24-20(15)16)13-4-6-14(21)7-5-13/h3-7,9-10,19,21-22H,8,11H2,1-2H3/t19-/m0/s1 |
| InChI Key | KYFBXCHUXFKMGQ-IBGZPJMESA-N |
| Use of | Isobavachin, an antioxidant isaolated from Psoralea morisiana with a prenyl group at position 8 of ring A, promotes neuronal differentiation and the potential role of its protein prenylation[1][2]. Properties Name Isobavachin Synonym More Synonyms Isobavachin Biological Activity Description Isobavachin, an antioxidant isaolated from Psoralea morisiana with a prenyl group at position 8 of ring A, promotes neuronal differentiation and the potential role of its protein prenylation[1][2]. Related Catalog Signaling Pathways >> Others >> Others Research Areas >> Neurological Disease References [1]. Wang DY, et al. Promoting effects of isobavachin on neurogenesis of mouse embryonic stem cells were associated with protein prenylation. Acta Pharmacol Sin. 2011 Apr;32(4):425-32. [2]. Antonella Rosa, et al. Antioxidant properties of extracts and compounds from Psoralea morisiana. European Journal of Lipid Science and Technology. 2005. Chemical & Physical Properties Molecular Formula C20H20O4 Exact Mass 324.136169 PSA 66.76000 Index of Refraction 1.622 InChIKey KYFBXCHUXFKMGQ-IBGZPJMESA-N Safety Information HS Code 2932999099 Synthetic Route Total: 1 Page GAMMA GAMMA-DIM... CAS#:358-72-5 Liquiritigenin CAS#:578-86-9 Isobavachin CAS#:31524-62-6 Literature: Advanced Synthesis and Catalysis, , vol. 355, # 9 p. 1817 - 1828 Precursor & DownStream Precursor 2 CAS#:358-72-5 GAMMA GAMMA-DIM... CAS#:578-86-9 Liquiritigenin DownStream 0 |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 20.0% |
| Transport Info | Product name: Summary 2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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