89763-86-0

Basic information

• Product Name: 1-[4-(TRIFLUOROMETHYL)PHENOXY]-2-PROPANAMINE
• Synonyms: 1-[4-(TRIFLUOROMETHYL)PHENOXY]-2-PROPANAMINE
• CAS NO: 89763-86-0
• Molecular Formula: C₁₀H₁₂F₃NO
• Molecular Weight: 219.2
• Mol File: 89763-86-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-[4-(TRIFLUOROMETHYL)PHENOXY]-2-PROPANAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[4-(TRIFLUOROMETHYL)PHENOXY]-2-PROPANAMINE(89763-86-0)
• EPA Substance Registry System: 1-[4-(TRIFLUOROMETHYL)PHENOXY]-2-PROPANAMINE(89763-86-0)

Safety Data

• Hazardous Substances Data: 89763-86-0(Hazardous Substances Data)

Usage

Propylamine derivative

A type of amine compound
This indicates that the compound is derived from propylamine, which is an organic compound containing an amine functional group (-NH2).

Trifluoromethyl group

A functional group with three fluorine atoms
The presence of a trifluoromethyl group (-CF3) attached to the phenoxy ring contributes to the compound's unique properties and reactivity.

Phenoxy ring

Aromatic ring structure

Intermediate in synthesis

Used in the production of pharmaceuticals and agrochemicals
1-[4-(TRIFLUOROMETHYL)PHENOXY]-2-PROPANAMINE serves as a building block or intermediate in the synthesis of various pharmaceuticals and agrochemicals, making it an important component in the development of new drugs and chemicals.

Therapeutic potential

Researched for use in treating medical conditions
The compound has been investigated for its potential therapeutic applications, suggesting that it may have beneficial effects on human health.

Physiological and pharmacological properties

Valuable in medicinal chemistry
The compound's physiological and pharmacological properties make it a valuable compound in the field of medicinal chemistry, as it may have potential applications in the development of new drugs and therapies.

Chemical structure

Contains an amine group, a phenoxy ring, and a trifluoromethyl group
The specific arrangement of these functional groups in the molecule contributes to its unique properties and potential applications in various fields.

Upstream product

• 1036762-58-9 C₁₀H₉F₃O₂ 
• 402-45-9 4-hydroxybenzotrifluoride 

Relevant articles and documents

A (different) bright ammonia amide carbamate derivative and application thereof (by machine translation)

The invention belongs to the field of plant, relates to a general formula (I) is shown in a (different) bright ammonia amide carbamate derivatives and their pharmaceutically acceptable salt, wherein substituent R has the definition given in the specification, the invention also relates to the general formula (I) preparation of compounds of the, specifically for the preparation of the intermediate of its development and application of plant disease control. (by machine translation)

Design, synthesis and effect of the introduction of a propargyloxy group on the fungicidal activities of 1-substituted phenoxypropan-2-amino valinamide carbamate derivatives

The cell walls of oomycetes are composed of cellulose, making cellulose synthase enzymes good targets for carboxylic acid amide fungicides. Valinamide carbamates are amino acid fungicides that represent excellent alternatives to conventional synthetic pesticides in terms of their ability to reduce the negative impacts of these compounds on human health and the environment. In a continuation of our research towards the development of new cellulose synthase inhibitors, we have developed a series of "stretched" analogues of iprovalicarb by the introduction of an additional OCH2 linker. The bioassay results indicated that compounds containing a small group at the para-position of phenyl gave excellent fungicidal activities with EC50 values ranging from 0.59 to 2.06 μmol L-1. Most notably, the introduction of a propargyloxy group led to a pronounced increase in the fungicidal activity. Furthermore, compound 7o bearing a propargyloxy group was identified as the most promising candidate because of its excellent fungicidal potency against oomycete diseases and good fungicidal activity against non-oomycete diseases.

NOVEL MICROBIOCIDES

Compounds of the formula (I), in which the substituents are as defined in claim 1 are suitable for use as microbiocides.