814254-62-1 Usage
Description
(1-aminocycloheptyl)methanol (SALTDATA: FREE) is a chemical compound with the formula C8H17NO, characterized by its molecular weight of 143.23 g/mol. This aminocycloheptyl derivative features a cyclic seven-membered ring with an amino group and a hydroxyl group attached to it. At room temperature, it exists as a white solid and is soluble in both water and organic solvents. It serves as a versatile building block in the synthesis of other compounds and is utilized in various chemical and pharmaceutical applications.
Uses
Used in Chemical Synthesis:
(1-aminocycloheptyl)methanol (SALTDATA: FREE) is used as a building block in chemical synthesis for the creation of a variety of compounds. Its unique structure and functional groups make it a valuable component in the development of new chemical entities.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, (1-aminocycloheptyl)methanol (SALTDATA: FREE) is used as a precursor in the synthesis of pharmaceuticals. Its ability to form stable compounds with other molecules makes it a promising candidate for the development of new drugs and therapeutic agents.
Used in Research and Development:
(1-aminocycloheptyl)methanol (SALTDATA: FREE) is also utilized in research and development settings, where its properties are studied and explored for potential applications in various fields. Its versatility and reactivity contribute to the advancement of scientific knowledge and innovation.
It is crucial to handle (1-aminocycloheptyl)methanol (SALTDATA: FREE) with care and adhere to safety guidelines when working with this chemical compound to ensure the safety of both individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 814254-62-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,4,2,5 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 814254-62:
(8*8)+(7*1)+(6*4)+(5*2)+(4*5)+(3*4)+(2*6)+(1*2)=151
151 % 10 = 1
So 814254-62-1 is a valid CAS Registry Number.
814254-62-1Relevant articles and documents
Design and Synthesis of Fsp3-Rich, Bis-Spirocyclic-Based Compound Libraries for Biological Screening
Stotani, Silvia,Lorenz, Christoph,Winkler, Matthias,Medda, Federico,Picazo, Edwige,Ortega Martinez, Raquel,Karawajczyk, Anna,Sanchez-Quesada, Jorge,Giordanetto, Fabrizio
, p. 330 - 336 (2016/07/06)
The exploration of innovative chemical space is a critical step in the early phases of drug discovery. Bis-spirocyclic frameworks occur in natural products and other biologically relevant metabolites and show attractive features, such as molecular compactness, structural complexity, and three-dimensional character. A concise approach to the synthesis of bis-spirocyclic-based compound libraries starting from readily available commercial reagents and robust chemical transformations has been developed. A number of novel bis-spirocyclic scaffold examples, as implemented in the European Lead Factory project, is presented.
Sterically demanding, bioxazoline-derived N-heterocyclic carbene ligands with restricted flexibility for catalysis
Altenhoff, Gereon,Goddard, Richard,Lehmann, Christian W.,Glorius, Frank
, p. 15195 - 15201 (2007/10/03)
A unique family of N-heterocyclic carbenes derived from bioxazolines (IBiox) suitable for application in transition-metal catalysis is described. The ligands are electron rich, sterically demanding, and have restricted flexibility. Their usefulness has been demonstrated in the Suzuki-Miyaura cross-coupling of sterically hindered aryl chlorides and boronic acids. For the first time, tetraortho-substituted biaryls with methyl and larger ortho-substituents have been synthesized from aryl chlorides using the Suzuki-Miyaura method.
