105827-84-7

Basic information

• Product Name: 2-[[(6-CHLORO-3-PYRIDINYL)METHYL]AMINO]-ETHANOL
• Synonyms: 2-[[(6-CHLORO-3-PYRIDINYL)METHYL]AMINO]-ETHANOL
• CAS NO: 105827-84-7
• Molecular Formula: C₈H₁₁ClN₂O
• Molecular Weight: 186.641
• Mol File: 105827-84-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-[[(6-CHLORO-3-PYRIDINYL)METHYL]AMINO]-ETHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[[(6-CHLORO-3-PYRIDINYL)METHYL]AMINO]-ETHANOL(105827-84-7)
• EPA Substance Registry System: 2-[[(6-CHLORO-3-PYRIDINYL)METHYL]AMINO]-ETHANOL(105827-84-7)

Safety Data

• Hazardous Substances Data: 105827-84-7(Hazardous Substances Data)

Usage

Chemical structure

2-[[(6-CHLORO-3-PYRIDINYL)METHYL]AMINO]-ETHANOL consists of a pyridine ring with a chlorine atom attached to the 6th position, connected to an amino group and an ethanol group.

Molecular composition

The compound is composed of carbon (C), hydrogen (H), chlorine (Cl), and nitrogen (N) atoms.

Pharmaceutical industry

It may have therapeutic effects due to its structure.

Agriculture

It has been studied for its potential use as a pesticide or herbicide.

Research status

Further research is needed to fully understand the properties and potential uses of this chemical compound.

Upstream product

• 70258-18-3 2-chloro-5-(chloromethyl)pyridine 
• 141-43-5 ethanolamine 
• 23100-12-1 6-chloronicotinylaldehyde 

Relevant articles and documents

Imidazopyridine compound, intermediate, preparation method and application thereof

The invention discloses an imidazopyridine compound represented by a formula (I), a preparation method and application thereof, wherein each substituent in the formula is defined in the specification.The compound represented by the formula (I) has insecticidal and bactericidal biological activity, particularly has high activity on pests such as aphids, plant hoppers and the like, and can be usedfor preventing and treating pests and diseases such as aphids, plant hoppers, sclerotiniose and the like. The technical scheme of the invention also comprises an intermediate for preparing the compound represented by the formula (I), wherein the structure of the intermediate is represented by a general formula (II), and each substituent in the formula is defined in the specification.

Synthesis, herbicidal activity, and structure-bioactivity relationship of pyridyl-containing 2-phenyliminothiazolidines

A series of novel 2-phenyliminothiazolidine derivatives were designed and synthesized. All title compounds were characterized by 1H NMR and, in some cases, by 13C NMR, IR, and HRMS. Their agricultural bioactivities were evaluated and some of these compounds exhibited efficient herbicidal activities against Echinochloa crusgalli, Sorghum vulgare, Digitaria sanguinalis, Eclipta prostrasta, Cucumis sativus, and Brassica campestris at 50∈μg/cm3. Analysis of the quantitative structure-activity relationship (QSAR) showed that the electronic parameter was the main factor to affect herbicidal activities.

INSECTICIDAL N-(HETEROARYLALKYL) ALKANEDIAMINE DERIVATIVES

Certain noel N-(heteroarylalkyl)alkanediamine derivatives have provided unexpected insecticidal and acaricidal activity. These compounds are represented by formula I: wherein Ar, a, r, R, R, R, R, R, b, c, R, R, R, R, R, d, e, U