13289-38-8 Usage
General Description
Ethyl 4-(carbamoylamino)benzoate is a chemical compound with the molecular formula C11H13NO4. It is a white crystalline solid, with a faint odor, and is commonly used as an intermediate in the production of pharmaceuticals and other organic compounds. This chemical is a derivative of benzoic acid and contains an ethyl ester group, a carbamoylamino group, and a benzene ring. It is mainly used as a building block in the synthesis of various drugs and pharmaceuticals, particularly those used to treat pain and inflammation. It is also used as a flavoring agent in the food and beverage industry. Ethyl 4-(carbamoylamino)benzoate is generally considered to be safe for use in these applications when handled and used according to proper safety guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 13289-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,8 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13289-38:
(7*1)+(6*3)+(5*2)+(4*8)+(3*9)+(2*3)+(1*8)=108
108 % 10 = 8
So 13289-38-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O3/c1-2-15-9(13)7-3-5-8(6-4-7)12-10(11)14/h3-6H,2H2,1H3,(H3,11,12,14)
13289-38-8Relevant articles and documents
Design and Synthesis of Iminosydnones for Fast Click and Release Reactions with Cycloalkynes
Riomet, Margaux,Decuypere, Elodie,Porte, Karine,Bernard, Sabrina,Plougastel, Lucie,Kolodych, Sergii,Audisio, Davide,Taran, Frédéric
supporting information, p. 8535 - 8541 (2018/05/30)
Emerging applications in the field of chemical biology are currently limited by the lack of bioorthogonal reactions allowing both removal and linkage of chemical entities on complex biomolecules. We recently discovered a novel reaction between iminosydnones and strained alkynes leading to two products resulting from ligation and fragmentation of iminosydnones under physiological conditions. We now report the synthesis of a panel of substituted iminosydnones and the structure reactivity relationship between these compounds and strained alkyne partners. This study identified the most relevant substituents, which allow to increase the rate of the transformation and to develop a bifunctional cleavable linker with improved kinetics.
