Building Blocks

1,2-Dipropoxybenzene is a colorless liquid with a pleasant odor. It is soluble in water and insoluble in alcohol. The compound has been shown to inhibit the growth of bacteria such as Bacillus subtilis and Escherichia coli at low concentrations. This compound also has strong interactions with other compounds, such as its reaction with 1,4-dichlorobenzene to form 2,4-dichlorobenzophenone. 1,2-Dipropoxybenzene is biodegradable and has been shown to have a low toxicity for both aquatic organisms and mammals. This compound crystallizes from hot water or ethanol solution at room temperature.br>br>
The structure of this molecule includes an aromatic ring that contains two benzene rings fused together with one oxygen atom between them. The three hydrogens on the benzene ring are not involved in any hydrogen bonding interactions; instead they are passively protonated by

Versatile small molecule scaffold

Versatile small molecule scaffold

2-Amino-5-methoxythiophenol is an organic compound that is used as a fluorescent probe for the measurement of mitochondrial membrane potential. The optimal reaction conditions are 3:1 methanol to water, with a reaction time of 10 minutes at room temperature. The demethylation of 2-amino-5-methoxythiophenol yields 3-mercaptopropionic acid, which can be used as a synthetic intermediate in other organic synthesis reactions. It has been found that the ring opening of 2-amino-5-methoxythiophenol occurs through oxidation and the formation of radicals. This reaction mechanism is supported by the photophysical properties observed in its fluorescence spectrum.

Versatile small molecule scaffold

N-Methyl-N-phenylprop-2-enamide is a perfluorinated compound with acrylate functional groups. It is a monomer that can react with other compounds to form polymers. It has been shown to be useful in the production of polyacrylates, which are used in industrial and medical applications. NMPEA has a bond cleavage reaction when it reacts with triphosgene, which can lead to the formation of acrylonitrile and chlorobenzene. This type of reaction also exhibits hydrogen bonding interactions and can be activated by an amide or an alcohol.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

4-(1,3-Benzothiazol-2-yl)phenol is an antibacterial agent that contains a methoxy group. It has been shown to have potent cytotoxicity against cancer cells and may be used for the treatment of cancer. 4-(1,3-Benzothiazol-2-yl)phenol is an oxidant that is able to form covalent bonds with proteins and other molecules through hydrogen bonding. The oxidation products of 4-(1,3-Benzothiazol-2-yl)phenol are also potent cytotoxins and inhibitors of bacterial growth. The molecular modeling studies on this compound indicate that it binds to DNA by intermolecular hydrogen bonding. This drug targets the enzyme thymidylate synthase, which catalyzes the conversion of dUMP to dTMP in the de novo pathway of DNA synthesis. 4-(1,3-Benzothiazol-2-yl)phenol has been

Versatile small molecule scaffold

2-Cyclopentylidenecyclopentan-1-ol is a cyclic ether with the chemical formula of C10H14O. It is a reactive, exploratory molecule that contains a hydrogenated, hydrochloric acid, and photolyzed dipole. This compound is a hydroxyl group with an epoxide that yields centrosymmetric molecules. 2-Cyclopentylidenecyclopentan-1-ol has been shown to have yields of 54%.

Versatile small molecule scaffold