17409-41-5 Usage
General Description
Glycolamide, N,N-bis(2-hydroxyethyl)- is a chemical compound that belongs to the class of glycolamides, which are known for their potential applications in various industries such as pharmaceuticals, cosmetics, and polymers. Glycolamide, N,N-bis(2-hydroxyethyl)- is formed by the reaction of glycolic acid with ammonia and ethylene oxide, resulting in a compound with two hydroxyethyl groups attached to the nitrogen atom. Glycolamide, N,N-bis(2-hydroxyethyl)- is commonly used as a chelating agent in metal ion complexation reactions and as a building block in the synthesis of polymers and other organic compounds. Additionally, this chemical may also have potential applications in the field of medicine, particularly in drug delivery systems and pharmaceutical formulations due to its ability to form stable complexes with certain drugs and enhance their solubility and bioavailability.
Check Digit Verification of cas no
The CAS Registry Mumber 17409-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,0 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17409-41:
(7*1)+(6*7)+(5*4)+(4*0)+(3*9)+(2*4)+(1*1)=105
105 % 10 = 5
So 17409-41-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO4/c8-3-1-7(2-4-9)6(11)5-10/h8-10H,1-5H2
17409-41-5Relevant articles and documents
Synthesis and evaluation of in vitro anti-tuberculosis activity of N-substituted glycolamides
Daryaee, Fereidoon,Kobarfard, Farzad,Khalaj, Ali,Farnia, Parisa
experimental part, p. 289 - 295 (2009/04/07)
On the basis of the structural similarity of N-substituted glycolamides with N-glycolyl muramic acid residues of the cell wall of Mycobacterium tuberculosis, a series of these compounds were designed and synthesized by the reaction of glycolic acid acetonide 1 (2,2-dimethyl-5-oxo-1,3-dioxolane) with the proper amines. The minimum inhibitory concentration (MIC) was determined against M. tuberculosis H37Rv in BACTEC 12B medium, using the Microplate Alamar Blue Assay (MABA). Among the synthesized compounds, all those with disubstituted amide structure accompanied by one or two heteroatom(s) with loan pair(s) of electrons atom(s) β to the amide nitrogen demonstrated moderate anti-tuberculosis activity and all the monosubstituted amides showed no activity at all.
