42287-87-6 Usage
Description
3-(3,5-DIMETHYLPHENYL)PROPANOIC ACID is a distinctive chemical compound characterized by the molecular formula C12H16O2. It is composed of a propanoic acid group, a basic carboxylic acid, connected to a phenyl ring substituted with two methyl groups at the 3rd and 5th positions. 3-(3,5-DIMETHYLPHENYL)PROPANOIC ACID is primarily utilized in chemical research and synthesis, owing to its unique molecular structure. However, it requires cautious handling and storage due to its potential hazards. 3-(3,5-DIMETHYLPHENYL)PROPANOIC ACID's physical properties, such as boiling point, melting point, and density, may exhibit slight variations depending on impurities and other factors.
Uses
Used in Chemical Research and Synthesis:
3-(3,5-DIMETHYLPHENYL)PROPANOIC ACID is used as a chemical intermediate for the synthesis of various compounds in chemical research. Its specific molecular structure makes it a valuable component in the development of new chemical entities and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(3,5-DIMETHYLPHENYL)PROPANOIC ACID is used as a building block for the creation of new drug molecules. Its unique structure can contribute to the design of novel therapeutic agents with potential applications in medicine.
Used in Material Science:
3-(3,5-DIMETHYLPHENYL)PROPANOIC ACID is employed as a component in the development of new materials with specific properties. Its incorporation into material compositions can lead to advancements in areas such as polymer science, coatings, and adhesives.
Used in Environmental Applications:
3-(3,5-DIMETHYLPHENYL)PROPANOIC ACID may be utilized in environmental applications, such as in the development of biodegradable materials or in processes that aim to reduce the environmental impact of certain chemical substances. Its use in these contexts is driven by the need for sustainable and eco-friendly solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 42287-87-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,8 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42287-87:
(7*4)+(6*2)+(5*2)+(4*8)+(3*7)+(2*8)+(1*7)=126
126 % 10 = 6
So 42287-87-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O2/c1-8-5-9(2)7-10(6-8)3-4-11(12)13/h5-7H,3-4H2,1-2H3,(H,12,13)
42287-87-6Relevant articles and documents
Aldehyde as a Traceless Directing Group for Regioselective C-H Alkylation Catalyzed by Rhodium(III) in Air
Chen, Si-Qi,Fan, Juan,Li, Chao-Jun,Li, Xin-Ran,Liu, Zhong-Wen,Shi, Xian-Ying
supporting information, p. 1259 - 1264 (2020/03/13)
The aromatic aldehyde as a traceless directing group for the regionselective C-H alkylation catalyzed by rhodium(III) under aerobic atmospheric conditions has been developed. The process involves an aldehyde assisted direct addition of C-H bond to unsaturated electrophiles of acrylates or acrylic acids, and the subsequent decarbonylation. A trace amount of water is found to favor the reaction.
An investigation into the tether length and substitution pattern of arene-substituted complexes for asymmetric transfer hydrogenation of ketones
Cheung, Fung K.,Lin, Changxue,Minissi, Franco,Criville, Adriana Lorente,Graham, Mark A.,Fox, David J.,Wills, Martin
, p. 4659 - 4662 (2008/03/12)
(Figure Presented) A series of Ru(II) catalysts were prepared and tested in the asymmetric transfer hydrogenation of ketones. The catalyst containing a "4-carbon" tether gave the fastest rates of ketone reduction. This is due to both increased rate of reg
