CAS 1129-46-0
:(R)-(+)-2-PHENOXYPROPIONIC ACID
Description:
(R)-(+)-2-Phenoxypropionic acid, with the CAS number 1129-46-0, is a chiral organic compound characterized by its phenoxy and propionic acid functional groups. It typically appears as a white to off-white crystalline solid and is soluble in organic solvents, while exhibiting limited solubility in water. This compound is known for its role as a herbicide, particularly in the selective control of certain broadleaf weeds in agricultural settings. The (R)-enantiomer is often more biologically active than its counterpart, which is significant in its application. Its molecular structure includes a phenoxy group attached to a propionic acid moiety, contributing to its herbicidal properties. Additionally, it may exhibit various biological activities, including potential effects on plant growth regulation. Safety and handling precautions are essential, as with many chemical substances, to mitigate any potential hazards associated with its use. Overall, (R)-(+)-2-Phenoxypropionic acid is an important compound in both agricultural and chemical research contexts.
Formula:C9H10O3
InChI:InChI=1/C9H10O3/c1-7(9(10)11)12-8-5-3-2-4-6-8/h2-7H,1H3,(H,10,11)/t7-/m1/s1
InChI key:InChIKey=SXERGJJQSKIUIC-SSDOTTSWSA-N
SMILES:C[C@H](C(=O)O)Oc1ccccc1
Synonyms:- (+)-2-Phenoxypropanoic acid
- (+)-2-Phenoxypropionic acid
- (2R)-2-phenoxypropanoic acid
- (R)-2-Phenoxypropanoic acid
- Propanoic acid, 2-phenoxy-, (2R)-
- Propanoic acid, 2-phenoxy-, (R)-
- Propionic acid, 2-phenoxy-, <span class="text-smallcaps">D</span>-
- R-Ppa
- (R)-2-PHENOXYPROPIONIC ACID
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Found 4 products.
(R)-(+)-2-Phenoxypropionic acid
CAS:Formula:C9H10O3Purity:98%Color and Shape:SolidMolecular weight:166.1739(R)-(+)-2-Phenoxypropionic acid
CAS:(R)-(+)-2-Phenoxypropionic acidPurity:98%Molecular weight:166.17g/mol(R)-2-Phenoxypropionic acid
CAS:Formula:C9H10O3Purity:98%Color and Shape:SolidMolecular weight:166.176(R)-2-PHENOXYPROPIONIC ACID
CAS:<p>(R)-2-PHENOXYPROPIONIC ACID is a reactive chemical that is used in process optimization to produce enantiopure amines. It is synthesized by the stereoselective addition of phenyl chlorides to aldehydes and ketones. The (R) form of 2-phenoxypropionic acid has been shown to be the most efficient method for the synthesis of amines with high yields, as well as being an efficient method for the production of amino acids. This compound can catalyze the decarboxylation of carboxylic acids, which may result in a more efficient synthesis of hydrocarbons. Process optimization also includes kinetic studies on (R)-2-phenoxypropionic acid and chloride ions, which have shown that this compound is reactive at room temperature with rates comparable to those found in solution at higher temperatures. The reaction mechanism for this compound involves the formation of an acid complex with two equivalents of HCl</p>Formula:C9H10O3Purity:Min. 95%Molecular weight:166.17 g/mol



