42287-87-6 Usage
General Description
3-(3,5-DIMETHYLPHENYL)PROPANOIC ACID is a unique chemical compound with the molecular formula C12H16O2. As suggested by its name, it features a propanoic acid group - a simple carboxylic acid - attached to a phenyl ring with two methyl groups in the 3rd and 5th positions. 3-(3,5-DIMETHYLPHENYL)PROPANOIC ACID can be used in a variety of applications, largely in chemical research and synthesis due to its specific molecular structure. However, like many chemicals, it necessitates careful handling and storage due to its potentially hazardous nature. The toxicity, environmental impact, and specific use-cases largely depend on the particular method of application and usage quantities. The precise physical properties of this compound, such as its boiling point, melting point, and density may vary slightly, based on impurities and other factors.
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