14155-86-3

Usage

Uses

1-BROMO-5-METHOXYPENTANE is used as a reagent for the preparation of benzobis(thiadiazole) derivatives with oxygen-containing hydrocarbon groups. These derivatives are essential components in the development of organic electronic devices, such as organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). The compound's unique structure allows for the formation of these derivatives, which exhibit improved performance and enhanced properties in electronic applications.
Used in Organic Electronic Devices Industry:
1-BROMO-5-METHOXYPENTANE is used as a key intermediate for the synthesis of benzobis(thiadiazole) derivatives with oxygen-containing hydrocarbon groups. These derivatives are crucial in the development of advanced organic electronic devices, such as OLEDs, OPVs, and OFETs, due to their improved performance and enhanced properties. The compound's reactivity and versatility make it an essential component in the synthesis of these materials, contributing to the advancement of organic electronics.

Upstream product

• 67-56-1 methanol 
• 111-24-0 1,5-dibromo-pentane 
• 124-41-4 sodium methylate 
• 4799-62-6 O-methyl-pentamethylene glycol 

Downstream Products

• 142-68-7 TETRAHYDROPYRANE 
• 100450-60-0 5-Methoxy-1-(4-nitro-2-methoxy-phenoxy)-pentan 
• 1185089-63-7 N-[4-(5-methoxypentyloxy)phenyl]methyl-2-aminonicotinic acid amide 
• 1202182-77-1 N-(3-(5-methoxypentyloxy)phenyl)methyl-benzothiazole-6-carboxamide 

Relevant academic research and scientific papers

BENZOBIS(THIADIAZOLE) DERIVATIVE CONTAINING OXYGEN-CONTAINING HYDROCARBON GROUP, INK CONTAINING THE SAME, AND ORGANIC ELECTRONICS DEVICE USING THE SAME

PROBLEM TO BE SOLVED: To provide a benzobis(thiadiazole) derivative providing an organic semiconductor ink excellent in migration rate of electrons (electric field effect migration rate), excellent in stability in air and having no generation of deposit at a room temperature. SOLUTION: There is provided a benzobis derivative represented by the formula (1). R1 to R4 are a C2 to 41 alkyl group substituted/unsubstituted by trifluoromethyl group, a cyano group, a trifluoromethoxy group, an alkyl group and having an ether bond in a chain, a C1 to 40 alkyl group or a C1 to 21 alkyl group having a phenyl group at a terminal and having an ether bond in a chain, one or more of R1 to R4 is the C1 to 40 alkyl group having the phenyl group at the terminal and having the ether bond in the chain. SELECTED DRAWING: Figure 8 COPYRIGHT: (C)2019,JPOandINPIT

AMINE COMPOUNDS HAVING ANTI-INFLAMMATORY, ANTIFUNGAL, ANTIPARASITIC AND ANTICANCER ACTIVITY

Amine compounds having activity against inflammation, fungi, unicellular parasitic microorganisms, and cancer are described. The compounds contain a monocyclic, bicyclic, or tricyclic aromatic ring having one, two, or three ring nitrogen atoms.

Hydrogen Bonds involving Polar CH Groups. Part 9. Optimum Structural Parameters, and Unequivocal Demonstration of such Intramolecular Interactions in 2-Substituted 1,3-Dithian 1,1,3,3-Tetraoxides

A series of 2-monosubstituted 1,3-dithian 1,1,3,3-tetraoxides have been prepared, having side chains with 2-6 carbon atoms, and bearing alkyl, aryl, methoxy, dialkylamino, and pyridyl terminal substituents, as models for intramolecular C-H...X hydrogen bonds.Methoxy- and amino-substituents, in compounds having two or three carbon atoms in the side chain, show significant intramolecular interaction with the disulphone methine hydrogen in dichloromethane, as evidenced by a downfield shift of the 1H n.m.r. signals; shifts of up to 2.0 p.p.m. have been observed.Intramolecular H-bonds are disrupted in acetone and in pyridine owing to competing intermolecular interactions with the solvents, and in trifluoroacetic acid owing to protonation of the donor atom.