25580-88-5 Usage
Uses
Used in Pharmaceutical Industry:
Hexanoic acid, 6-[[1-oxo-6-[[(phenylmethoxy)carbonyl]amino]hexyl]amino]-, methyl ester is used as an intermediate in the synthesis of 6-(6-(6-aminohexanamido)hexanamido)hexanoic acid (A618823) for the pharmaceutical industry. A618823 is a key component in the making of a preconjugate, which serves as an immunoreactive conjugate useful as a developer antigen in a competitive inhibition immunoassay for the detection of polymorphic analytes.
Used in Chemical Synthesis:
In the field of chemical synthesis, Hexanoic acid, 6-[[1-oxo-6-[[(phenylmethoxy)carbonyl]amino]hexyl]amino]-, methyl ester is utilized in the efficient synthesis of a heterobifunctional coupling agent. This agent plays a crucial role in the formation of covalent bonds between different molecules, which is essential for the development of various chemical products and materials.
Used in Research and Development:
Hexanoic acid, 6-[[1-oxo-6-[[(phenylmethoxy)carbonyl]amino]hexyl]amino]-, methyl ester is also employed in research and development for its potential applications in the creation of new compounds and materials. Its unique molecular structure allows for further modification and exploration of its properties, which could lead to the discovery of novel applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 25580-88-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,8 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 25580-88:
(7*2)+(6*5)+(5*5)+(4*8)+(3*0)+(2*8)+(1*8)=125
125 % 10 = 5
So 25580-88-5 is a valid CAS Registry Number.
25580-88-5Relevant academic research and scientific papers
SYNTHESIS OF AZA-CROWN COMPOUNDS BY INTRAMOLECULAR CYCLIZATION OF ω-AMINO ACIDS
Mikhura, I. V.,Formanovskii, A. A.
, p. 205 - 212 (2007/10/02)
A method for the synthesis of aza-crown compounds by the intramolecular cyclization of ω-amino acids with subsequent reduction of the lactam to a macrocyclic amine was developed. 1,8-Diazacyclotetradecane and 1,8-dioxa-4,11-diazacyclotetradecane was synthesized in preparative yields.The structural assignments were made using the IR, 1H and 13C NMR, and mass spectra.
