35115-76-5

Basic information

• Product Name: 2,3-dichloro-3-phenyl-propanoic acid
• Synonyms: 2,3-dichloro-3-phenyl-propanoic acid
• CAS NO: 35115-76-5
• Molecular Formula: C₉H₈Cl₂O₂
• Molecular Weight: 219.06
• Mol File: 35115-76-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 312.1°Cat760mmHg
• Flash Point: 142.5°C
• Appearance: /
• Density: 1.392g/cm³
• Vapor Pressure: 0.000231mmHg at 25°C
• Refractive Index: 1.57
• CAS DataBase Reference: 2,3-dichloro-3-phenyl-propanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-dichloro-3-phenyl-propanoic acid(35115-76-5)
• EPA Substance Registry System: 2,3-dichloro-3-phenyl-propanoic acid(35115-76-5)

Safety Data

• Hazardous Substances Data: 35115-76-5(Hazardous Substances Data)

Usage

General Description

2,3-dichloro-3-phenyl-propanoic acid is a chemical compound with the molecular formula C9H7Cl2O2. It is a derivative of propionic acid and contains two chlorine atoms and a phenyl group attached to the carbon atom. 2,3-dichloro-3-phenyl-propanoic acid is commonly used in the synthesis of other chemicals and pharmaceuticals. It is also known for its ability to inhibit the growth of certain microorganisms and has potential applications in the field of medicine and agriculture. Due to its chemical properties and structure, 2,3-dichloro-3-phenyl-propanoic acid is important in various industrial and scientific processes.

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

Downstream Products

• 1727-39-5 α-chloro β-phenyl acrylic acid 
• 35115-84-5 Methyl α,β-dichloro-β-phenylpropionate 
• 87439-84-7 ethyl 2,3-dichloro-3-phenylpropenoate 
• 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 
• 74305-87-6 α-chloro-cinnamic acid anilide 
• 74305-85-4 α-chloro-cis-cinnamic acid amide 

Relevant articles and documents

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.

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