25173-68-6

Usage

Uses

Given the limited information provided on the usage or hazardous effects of 3-(3,4-Dichlorophenyl)propionic Acid, it is challenging to list its applications. However, based on its chemical properties, it can be inferred that it may have potential uses in various industries, such as:
Used in Chemical Synthesis Industry:
3-(3,4-Dichlorophenyl)propionic Acid is used as a building block or intermediate for the synthesis of more complex organic compounds, taking advantage of its reactivity and the presence of functional groups.
Used in Pharmaceutical Industry:
3-(3,4-Dichlorophenyl)propionic Acid may be used as a precursor in the development of new drugs, given its potential to form various derivatives through substitution reactions.
Used in Agrochemical Industry:
3-(3,4-Dichlorophenyl)propionic Acid could be employed as a starting material for the synthesis of agrochemicals, such as herbicides or pesticides, due to its reactivity and the possibility of forming active ingredients.

Upstream product

• 6582-42-9 1-(3,4-dichlorophenyl)propan-1-one 
• 1202-39-7 3,4-dichlorocinnamic acid 
• 7312-27-8 3,4-Dichlorocinnamic acid 
• 20595-44-2 3-(2,3-dichlorophenyl)acrylic acid 
• 95-50-1 1,2-dichloro-benzene 
• 115706-16-6 methyl 2-bromo-3-(3,4-dichlorophenyl)propionate 
• 95-76-1 m,p-dichloroaniline 
• 6287-38-3 3,4-dichlorobenzaldehyde 
• 115706-17-7 methyl 3‐(3,4‐dichlorophenyl)propanoate 

Downstream Products

• 39960-05-9 3-(3 ,4-dichlorophenyl)propan-1-ol 
• 39960-04-8 3-(3,4-dichlorophenyl)propionamide 
• 1027193-46-9 (S)-2-[3-(3,4-Dichloro-phenyl)-propionylamino]-N-(2-oxo-tetrahydro-thiophen-3-yl)-3-phenyl-propionamide 
• 115706-17-7 methyl 3‐(3,4‐dichlorophenyl)propanoate 
• 115706-19-9 6,7-dichloro-1,2,3,4-tetrahydro-1-oxoisoquinoline 
• 115706-18-8 1,2-dichloro-4-(2-isocyanatoethyl)benzene 
• 39960-06-0 4-(3,4-dichlorophenyl)butanenitrile 
• 76706-60-0 3-(3,4-dichlorophenyl)propan-1-amine 
• 732189-89-8 4-(3,4-dichlorophenyl)butan-1-amine 
• 101724-05-4 3-(3,4-dichlorophenyl)propanenitrile 
• 101282-76-2 3-<3,4-Dichlor-phenyl>-propyl-thiocarbamidsaeure-phenylester 
• 68755-31-7 5,6-dichloro-2,3-dihydro-1H-inden-1-one 
• 68755-30-6 6,7-dichloro-1-indanone 
• 1075623-25-4 N,N'-pentane-1,5-diylbis[3-(3,4-dichlorophenyl)propanamide] 

Relevant academic research and scientific papers

Benzo-aza-alkyl aryl piperazine derivative and applications in preparation of drugs

The invention discloses a benzo-aza-alkyl aryl piperazine derivative and applications in preparation of drugs. The derivative shows the effect on central nervous systems, especially on the double highaffinity activity of a 5-HT acceptor and a Sigma-1 acceptor. Various physiological and pharmacological effects are brought into play in the body; and the compound can be used as a pharmaceuticalactive substance, especially used for anti-depression, anti-anxiety, anti-bipolar affective disorder and anti-neuropathic pain, and can also be used as an intermediate to prepare other pharmaceuticalactive compounds. The compound is fast in effect and small in toxic and side effect, and can meet demands of clinical applications; and the compound is a compound or a free base or salt thereof havingthe following structural formula (IV). The structure of the compound or the free base or salt thereof is shown as the structural formula (IV).

Derivatives of 5H, 10H-imidazo[1, 2-a]indeno[1,2-e]pyrazin-4-one, preparation thereof and medicaments containing them

Compounds having the formula (I) wherein R and R 1, similar or different, represent a hydrogen or halogen atom or a radical alkyl, alkoxy, amino, acylamino, phenylureido, --N CH--N(R 2)R 3, nitro, imidazolyl, phenyl, SO 3 H or cyano; R 2 and R 3 which may

SUBSTITUTED HYDROXYUREAS

The present invention relates to substituted hydroxyureas. These compounds inhibit the enzyme 5-lipoxygenase. In addition, certain of the compounds also inhibit the enzyme-cyclooxygenase. The compounds are useful for treating asthma, allergies, arthritis, posoriasis, ischemia, dermatitis, inflammation and/or broncho-constriction and/or inflammatory diseases of the eye.

Synthesis and Antileukemic Activity of Bismethyl>-Substituted Pyrroloisoquinolines, Pyrroloquinolines, Pyrroloisobenzazepines, and Pyrrolobenzazepines

A series of bismethyl>-substituted pyrrole-fused tricyclic heterocycles were synthesized by using 1,3-dipolar cycloaddition reactions with a trifluoromethanesulfonate salt of an appropriate Resissert compound or with a mesoionic oxazolone intermediate.All of the bis(carbamates) were active in vivo against P388 lymphocytic leukemia with 5,6-dihydro-8-methoxy-1,2-bis(hydroxymethyl)pyrroloisoquinoline bis (3c) showing the highest level of activity.