494-19-9
494-19-9
Chemical Structure
Iminodibenzyl
- CAS No.: 494-19-9
- Formula:C14H13N
- Molecular Weight:195.26
IUPAC Name: 10,11-dihydro-5H-dibenzo[b,f]azepine
InChIKey: ZSMRRZONCYIFNB-UHFFFAOYSA-N
SMILES: C12=CC=CC=C1CCC3=CC=CC=C3N2
Biological Activity: Iminodibenzyl is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Iminodibenzyl | 99.98% | Iminodibenzyl is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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9-Aminophenanthrene | 99.74% | 9-Aminophenanthrene is a type of polycyclic aromatic amine compound, which can be used as a fluorescent labeling reagent for free fatty acids (FFA). | ||||||||||||||||||||
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Iminostilbene (Standard) | ≥98% | Iminostilbene (Standard) is the analytical standard of Iminostilbene. This product is intended for research and analytical applications. Iminostilbene is a a chemical precursor of carbamazepine. | ||||||||||||||||||||
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3,4-Dihydroquinolin-2(1H)-one | 3,4-Dihydroquinolin-2(1H)-one is a building block, that can be used for synthesis of antipsychotic agent, such as Aripiprazole (HY-14546) or CYP11B2 inhibitors. | |||||||||||||||||||||
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2-Benzylaniline | 2-Benzylaniline is an intermediate. 2-Benzylaniline can be used to synthesize Compound 15. Compound 15 shows an affinity for the D3 receptor with a Ki of 4654 nM. 2-Benzylaniline can be used in research on mental illnesses. | |||||||||||||||||||||
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9,10-Dihydrophenanthrene | 9,10-Dihydrophenanthrene is an analogue of 9,10-Phenanthrenequinone (HY-W014507). 9,10-Dihydrophenanthrene loses its anti-tumor activity that induces apoptosis in HCT-116 and HL-60 tumor cells. | |||||||||||||||||||||
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Dihydroanthracene | 99.63% | Dihydroanthracene (9,10-Dihydroanthracene) is a substrate for toluene dioxygenase (TDO) expressed by Pseudomonas putida UV4. Toluene dioxygenase (TDO) expressed by Pseudomonas putida UV4 catalyzes the benzylic monooxygenation of Dihydroanthracene to 9-hydroxy-9,10-DHA as the only product. | ||||||||||||||||||||
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9-Anthracenamine | 9-anthracenamine is an end-capping agent. 9-anthracenamine caps both ends of polyrotaxanes and free PPG chains to avoid dethreading. | |||||||||||||||||||||
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9,10-Dihydroacridine | 99.75% | 9,10-Dihydroacridine is a chain-terminating antioxidant that can inhibit lipid peroxidation by capturing peroxide free radicals (LOO•). | ||||||||||||||||||||
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1,2-Dihydroacenaphthylene-13C6 | 1,2-Dihydroacenaphthylene-13C6 is the 13C-labeled 1,2-Dihydroacenaphthylene. | |||||||||||||||||||||
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Indoline | 99.89% | Indoline is a derivative of Indole (HY-W001132). Indoline can use as the basic structure for CD4 mimetic compounds (CD4mcs), which triggers conformational changes of the HIV-1 envelope glycoprotein (Env) in advance, and causes viral inactivation. Indoline binds to gp120. Indoline CD4mcs can inhibit HIV-1AD8 with an IC50 in the micromolar range. | ||||||||||||||||||||
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