38446-21-8 Usage
Description
Ethyl 2-(ethylamino)benzoate is a yellowish solid with a fruity grape aroma. It is known for its medium strength odor and floral type fragrance. This chemical compound is characterized by its unique chemical properties and aroma profile, making it a versatile substance for various applications.
Uses
Used in Flavor and Fragrance Industry:
Ethyl 2-(ethylamino)benzoate is used as a flavoring agent for its fruity grape aroma, adding a pleasant taste to various food and beverage products. Its medium strength odor and floral type fragrance also make it a suitable candidate for use in the perfumery and cosmetics industry, where it can be used to create captivating and long-lasting scents.
Used in Pharmaceutical Industry:
Ethyl 2-(ethylamino)benzoate can be utilized as an active pharmaceutical ingredient or as a component in the development of new drugs. Its unique chemical properties may contribute to the treatment or management of specific medical conditions, making it a valuable asset in the pharmaceutical sector.
Used in Chemical Research:
Due to its distinct chemical properties, ethyl 2-(ethylamino)benzoate can be employed in various research applications, such as the synthesis of new compounds, the study of chemical reactions, or the development of novel materials. Its versatility in this field can lead to advancements in science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 38446-21-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,4 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38446-21:
(7*3)+(6*8)+(5*4)+(4*4)+(3*6)+(2*2)+(1*1)=128
128 % 10 = 8
So 38446-21-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO2/c1-3-12-10-8-6-5-7-9(10)11(13)14-4-2/h5-8,12H,3-4H2,1-2H3
38446-21-8Relevant articles and documents
Palladium-catalyzed oxidative carbonylation of aromatic C-H bonds of N -alkylanilines with CO and alcohols for the synthesis of o -aminobenzoates
Chen, Ming,Ren, Zhi-Hui,Wang, Yao-Yu,Guan, Zheng-Hui
, p. 1258 - 1263 (2015/01/30)
A Pd(II)-catalyzed C-H monocarbonylation of N-alkylanilines for the synthesis of o-aminobenzoates has been developed. Various aliphatic alcohols and phenol were tolerated in the reaction to afford the corresponding o-aminobenzoates in good yields under mild balloon pressure of CO.
Reactions of Anthranilium Salts with Nucleophiles: Adduct Formation and Rearrangement
Vander Meer, Robert K.,Olofson, R. A.
, p. 3373 - 3377 (2007/10/02)
3-Unsubstituted anthranilium salts 1 react with alcohols in the presence of bases to yield adducts 5 which rearrange to the esters 4 when refluxed in xylene.Similar processes involving 1 and cyanide or azide also have been observed.Evidence favoring benzoazetinones 2 as rearrangement intermediates is presented.The chemistry of 1 with phosphines and phosphites is also described.For example, treatment of 1c with trimethyl phosphite yields the rearranged adduct salt 14 which cleaves to the acyl phosphonate 15 when treated with triethylamine.
