99363-25-4 Usage
Description
TRANS-1,2-CYCLOPENTANEDIAMINE HYDROCHLORIDE is a chemical compound that serves as a salt form of cyclopentanediamine, featuring a five-membered ring with two amine groups. It is widely utilized in organic synthesis and pharmaceutical research, acting as a fundamental building block for the development of various pharmaceutical compounds.
Uses
Used in Pharmaceutical Research and Development:
TRANS-1,2-CYCLOPENTANEDIAMINE HYDROCHLORIDE is used as a key intermediate in the synthesis of pharmaceutical compounds for its ability to form essential molecular structures. Its presence in the molecular composition allows for the creation of diverse medicinal agents.
Used in Organic Synthesis:
In the field of organic synthesis, TRANS-1,2-CYCLOPENTANEDIAMINE HYDROCHLORIDE is used as a versatile building block for the creation of a broad spectrum of organic compounds, contributing to the advancement of chemical research and product development.
Used in Dye and Pigment Manufacturing:
TRANS-1,2-CYCLOPENTANEDIAMINE HYDROCHLORIDE is also utilized in the manufacturing of dyes and pigments, where its chemical properties contribute to the production of a variety of colorants for different applications.
Overall, TRANS-1,2-CYCLOPENTANEDIAMINE HYDROCHLORIDE is a multifaceted chemical compound with significant applications across the pharmaceutical, chemical, and dye industries, showcasing its importance in modern scientific and industrial processes.
Check Digit Verification of cas no
The CAS Registry Mumber 99363-25-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,6 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 99363-25:
(7*9)+(6*9)+(5*3)+(4*6)+(3*3)+(2*2)+(1*5)=174
174 % 10 = 4
So 99363-25-4 is a valid CAS Registry Number.
99363-25-4Relevant articles and documents
Synthesis of two stereoisomeric polydentate ligands, trans and cis cyclopentane-1,2-diaminotetraacetic acids, and complexation by 111In and 153Sm
Gouin, Sébastien G,Gestin, Jean-Fran?ois,Joly, Kevin,Loussouarn, Anthony,Reliquet, Alain,Claude Meslin, Jean,Deniaud, David
, p. 1131 - 1136 (2007/10/03)
Two polyaminocarboxylic acid chelating agents were synthesized. Complexation properties regarding 111In and 153Sm, two radionuclides suitable for applications in immunoscintigraphy and radioimmunotherapy were investigated. The synthesis of aminodiacetic acid derivatives 7a and 7b involved preliminary stereoselective synthesis of the corresponding amines, cis and trans cyclopentane-1,2-diamines. 111In labelling confirmed the complexation abilities of the two ligands. An additional comparative study to probe the relationship between ligand structure and metal complex was performed with 153Sm.
A short synthesis of trans-cyclopentane-1,2-diamine
Ongeri, Sandrine,Aitken, David J.,Husson, Henri-Philippe
, p. 2593 - 2597 (2007/10/03)
A convenient and rapid synthesis of the title compound is described, requiring three steps with no chromatographic purification; the key procedure is a double Curtius rearrangement.
