35115-76-5

Usage

Uses

Used in Pharmaceutical Synthesis:
2,3-dichloro-3-phenyl-propanoic acid is utilized as an intermediate in the synthesis of various pharmaceuticals for its ability to be chemically modified and incorporated into the structures of different medicinal compounds.
Used in Chemical Synthesis:
In the chemical industry, 2,3-dichloro-3-phenyl-propanoic acid is used as a building block for the creation of a range of other chemical compounds, leveraging its reactive sites for further functionalization.
Used in Antimicrobial Applications:
2,3-dichloro-3-phenyl-propanoic acid is employed as an antimicrobial agent, capitalizing on its ability to inhibit the growth of certain microorganisms, which is beneficial in both medical and agricultural settings for controlling infections and diseases.
Used in Agricultural Chemicals:
In agriculture, 2,3-dichloro-3-phenyl-propanoic acid is used as a component in the development of pesticides and other agrochemicals, where its antimicrobial properties contribute to crop protection and disease management.
Used in Scientific Research:
Due to its unique chemical structure and properties, 2,3-dichloro-3-phenyl-propanoic acid is important in various scientific research processes, where it may be studied for its reactivity, potential new applications, or as a model compound in chemical education and experimentation.

InChI:InChI=1/C9H8Cl2O2/c10-7(8(11)9(12)13)6-4-2-1-3-5-6/h1-5,7-8H,(H,12,13)

Upstream product

• 621-82-9 Cinnamic acid 
• 140-10-3 (E)-3-phenylacrylic acid 
• 67-56-1 methanol 
• 7791-25-5 sulfuryl dichloride 
• 20473-36-3 2,3-dichloro-3-phenyl-propionaldehyde 
• 7697-37-2 nitric acid 
• 7647-01-0 hydrogenchloride 
• 90649-87-9 2-chloro-3-hydroxy-3-phenyl-propionic acid 
• 140-10-3 cis-cinnamic acid 
• 7664-93-9 sulfuric acid 
• 7732-18-5 water 
• 7782-50-5 chlorine 
• 56-23-5 tetrachloromethane 
• 102-92-1 cinnamoyl chloride 

Downstream Products

• 1727-39-5 α-chloro β-phenyl acrylic acid 
• 35115-84-5 Methyl α,β-dichloro-β-phenylpropionate 
• 622-25-3 1-(2-chlorovinyl)benzene 
• 705-54-4 (Z)-α-chlorocinnamic acid 
• 705-55-5 (E)-2-chloro-3-phenylacrylic acid 
• 1674-29-9 (1,2,2-trichloro-ethyl)-benzene 
• 621-82-9 Cinnamic acid 
• 501-52-0 3-Phenylpropionic acid 
• 74305-85-4 α-chloro-cis-cinnamic acid amide 
• 74305-87-6 α-chloro-cinnamic acid anilide 
• 87439-84-7 ethyl 2,3-dichloro-3-phenylpropenoate 

Relevant academic research and scientific papers

Vicinal dichlorination of olefins using NH4Cl and oxone

A mild and efficient protocol for the preparation of 1,2-dichloroalkane derivatives from olefins using NH4Cl and Oxone at room temperature is described. A variety of terminal, internal, and cyclic alkenes reacted smoothly to give the corresponding dichlorinated products in good to excellent yields. Moreover, 1,2-disubstituted symmetrical and unsymmetrical olefins dichlorinated with moderate to excellent diastereoselectivity. This method precludes the use of acidic additives and transition metals in the synthesis of vicinal dichlorides.

Trichloroisocyanuric/TEMPO oxidation of alcohols under mild conditions: A close investigation

Efficient oxidation of primary alcohols to the corresponding carboxylic acids can be carried out at room temperature and in acetone/water, using trichloroisocyanuric acid (TCCA) in the presence of catalytic TEMPO. The mild conditions of this procedure and the total absence of any transition metal make this reaction suitable for safe laboratory use. A possible mechanism is presented and discussed.

AFM ON CHEMICALLY REACTING CRYSTALS

A review is given on recent developments of atomic force microscopic (AFM) studies on chemically reacting organic crystals.Three further basic phase transformation mechanisms have been added to the previous five.Both photodimerizations and gas/solid reactions are studied in detail by scanning the surfaces of initial and chemically reacted crystals of anthracenes, thiohydantoines, α- and β-cinnamic acid, and stilbene at different faces, where technically possible.The AFM-features are correlated to known crystal structure data with the aid of semiempirical calculations in part.Thus, detailed molecular mechanisms for the far-reaching well-directed transport phenomena may be derived in most cases and the appearance of the submicroscopic features rationalized.Unimolecular terrace steps of anthracene behave as independent crystal face already.The addition of bromine and chlorine leads to new solid phases directly even though there might be formed mixtures of stereoisomers.If a submicroscopic liquid phase is formed as in the reaction of α-cinnamic acid with chlorine, the surface will be remodelled by the tip and this provides for interesting nanostructures.In many cases there are secondary phase transformations apparently from one form of mixed crystals into another form of mixed crystals either upon continuation of irradiation or just on standing of gas/solid reacted crystals for several hours. - Keywords: atomic force microscopy, solid state photochemistry, gas/solid reaction, basic mechanism, phase transformation, molecular mechanism, unimolecular step, crystal face, crystal structure, nanostructures