(3aS)-3,3a,7,7aβ-Tetrahydro-3aβ-hydroxybenzofura-6(2H)-one
Cleroindicin F
CAS: 189264-47-9
Molecular Formula: C8H10O3
(3aS)-3,3a,7,7aβ-Tetrahydro-3aβ-hydroxybenzofura-6(2H)-one - Names and Identifiers
(3aS)-3,3a,7,7aβ-Tetrahydro-3aβ-hydroxybenzofura-6(2H)-one - Physico-chemical Properties
| Molecular Formula | C8H10O3 |
| Molar Mass | 154.16 |
| Density | 1.361±0.06 g/cm3(Predicted) |
| Boling Point | 332.9±42.0 °C(Predicted) |
| Specific Rotation(α) | ?2.7 (c, 0.02 in MeOH) |
| Appearance | oily |
| pKa | 12.88±0.20(Predicted) |
| Storage Condition | 2-8℃ |
(3aS)-3,3a,7,7aβ-Tetrahydro-3aβ-hydroxybenzofura-6(2H)-one - Introduction
Cleroindicin F(Cleroindicin F) is a naturally occurring pigment that belongs to the aflatoxin family. It is a colorless crystalline solid that exhibits a yellow color when dissolved in an organic solvent such as dimethyl sulfoxide or chloroform.
Cleroindicin F is mainly used as a biomarker for fluorescence microscopy and cell imaging studies. It can be combined with many biological molecules (such as proteins, nucleic acids and organelles) to make them visible and quantitatively analyzed.
Cleroindicin F can usually be obtained by synthesis or extraction from Aspergillus flavus fungi. Synthetic methods can use organic synthetic chemistry to synthesize its structurally related compounds and make specific modifications to them. Extraction from fungi can be accomplished by concentrating the extract, separating and purifying the extract.
There is no clear toxicity data and safety assessment regarding the safety of Cleroindicin F. However, appropriate safety measures need to be taken for the use of any chemical. It is recommended to wear appropriate personal protective equipment when using it and ensure that the operation is carried out in a well-ventilated area. Before use, should be carefully read and in accordance with the relevant instructions for use and experimental procedures for operation.
Cleroindicin F is mainly used as a biomarker for fluorescence microscopy and cell imaging studies. It can be combined with many biological molecules (such as proteins, nucleic acids and organelles) to make them visible and quantitatively analyzed.
Cleroindicin F can usually be obtained by synthesis or extraction from Aspergillus flavus fungi. Synthetic methods can use organic synthetic chemistry to synthesize its structurally related compounds and make specific modifications to them. Extraction from fungi can be accomplished by concentrating the extract, separating and purifying the extract.
There is no clear toxicity data and safety assessment regarding the safety of Cleroindicin F. However, appropriate safety measures need to be taken for the use of any chemical. It is recommended to wear appropriate personal protective equipment when using it and ensure that the operation is carried out in a well-ventilated area. Before use, should be carefully read and in accordance with the relevant instructions for use and experimental procedures for operation.
Last Update：2024-04-09 21:54:55
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Product Name: Cleroindicin F Visit Supplier Webpage Request for quotation
CAS: 189264-47-9
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 189264-47-9
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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