193483-62-4 Usage
Chemical structure
A complex chemical compound with multiple functional groups, consisting of a benzene ring with two carboxamide groups attached, as well as two hydroxypropyl groups and an oxo-2-pentylaminoethoxy group.
Molecular weight
411.51 g/mol
Functional groups
Carboxamide, hydroxypropyl, oxo-2-pentylaminoethoxy
Potential applications
May have applications in various industries, including pharmaceuticals, polymers, and materials science, due to its potential for forming complex structures and interactions with other molecules.
Further research
Further research and analysis are required to fully understand the properties and potential uses of this chemical.
It's important to note that this is a complex chemical compound and its properties and potential uses may vary depending on the specific context and conditions in which it is used. Further research and analysis are required to fully understand its properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 193483-62-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,4,8 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 193483-62:
(8*1)+(7*9)+(6*3)+(5*4)+(4*8)+(3*3)+(2*6)+(1*2)=164
164 % 10 = 4
So 193483-62-4 is a valid CAS Registry Number.
193483-62-4Relevant academic research and scientific papers
Synthesis and Hydrolytic Lability of α-Phenoxyacetamides Containing Hydroxy Groups in the N-alkyl Residue
Anelli, Pier Lucio,Brocchetta, Marino,Canipari, Sonia,Losi, Pietro,Manfredi, Giuseppe,et al.
, p. 135 - 142 (2007/10/03)
Secondary and tertiary amides of 3,5-biscarbonyl>phenoxyacetic acid bearing hydroxy groups in positions β (β-OH) and γ (γ-OH) relative to the acetamide nitrogen atom have been synthesized.Such amides easily undergo cleavage of the acetamide bond in water at neutral pH.Hydrolysis rate constant for a series of such amides and protonation constants for the corresponding leaving amines were determined.No simple correlation between the two parameters could be found.A study of the dependence of these parameters on the structural features of the substrates, such as the presence of an N-methyl group and number of β-OH and γ-OH groups, was carried out.All these features lead to enhancement of the amide hydrolysis rate and a synergistic effect is operative when both N-methyl and β-OH groups are contained in the substrate.Presence of a methyl group increases the basicity of amines whereas β-OH and γ-OH groups have the opposite effect.Mechanistic speculations seem to indicate that the abnormal lability of the acetamide bond is due to protic-like catalysis by an intramolecular OH...N hydrogen bond.
