100117-62-2 Usage
General Description
Ethyl 3,5-dimethylbenzoylformate, also known as ethyl 3,5-dimethylbenzoate, is a white to light yellow liquid with a fruity odor. It is commonly used as a flavoring agent in the food and beverage industry due to its fruity aroma. Additionally, it is also used as a fragrance ingredient in perfumes and cosmetic products. Ethyl 3,5-dimethylbenzoylformate is synthesized through the reaction of ethyl formate with 3,5-dimethylbenzoyl chloride, and it is considered safe for use in various consumer products. However, it should be handled and stored with proper care due to its flammability and potential health hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 100117-62-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,1 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100117-62:
(8*1)+(7*0)+(6*0)+(5*1)+(4*1)+(3*7)+(2*6)+(1*2)=52
52 % 10 = 2
So 100117-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O3/c1-4-15-12(14)11(13)10-6-8(2)5-9(3)7-10/h5-7H,4H2,1-3H3
100117-62-2Relevant articles and documents
Chiral Frustrated Lewis Pairs Catalyzed Highly Enantioselective Hydrosilylations of 1,2-Dicarbonyl Compounds
Ren, Xiaoyu,Du, Haifeng
supporting information, p. 810 - 813 (2016/02/09)
A highly enantioselective hydrosilylation of 1,2-dicarbonyl compounds was successfully realized for the first time utilizing the combination of tricyclohexylphosphine and chiral alkenylborane derived in situ from diyne as a frustrated Lewis pair catalyst. A variety of optically active α-hydroxy ketones and esters were obtained in 52-98% yields with 86-99% ee's.
Directing-group-assisted copper-catalyzed olefinic trifluoromethylation of electron-deficient alkenes
Feng, Chao,Loh, Teck-Peng
supporting information, p. 122414 - 122417 (2013/12/04)
Assistance provided: The directing group in the title reaction not only activates the substrates but also allows the stereospecific formation of cis-trifluoromethylated products. The reaction is operationally simple and tolerates a wide variety of functional groups, thus providing an efficient method for the stereoselective synthesis of β-CF3-functionalized acrylamide derivatives. Copyright
