4441-59-2 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
4-Cyclohexyl-butylamine is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals for its ability to contribute to the formation of complex organic molecules that possess desired therapeutic or pesticidal properties.
Used as a Corrosion Inhibitor:
4-Cyclohexyl-butylamine serves as a corrosion inhibitor, protecting metal surfaces from degradation in various industrial applications, thereby extending the lifespan of equipment and reducing maintenance costs.
Used as a Reagent in Organic Synthesis:
In the realm of organic synthesis, 4-Cyclohexyl-butylamine is employed as a reagent, facilitating specific chemical reactions that are crucial for the production of a range of organic compounds.
Used in Polymer Production:
4-Cyclohexyl-butylamine has potential applications in the production of polymers, where it may be used to modify polymer properties or as a component in the synthesis of specialty polymers with unique characteristics.
Used as a Surfactant in Industrial Processes:
4-CYCLOHEXYL-BUTYLAMINE also functions as a surfactant in various industrial processes, enhancing the efficiency of emulsions, dispersions, and other processes where the reduction of surface tension is beneficial.
Check Digit Verification of cas no
The CAS Registry Mumber 4441-59-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,4 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4441-59:
(6*4)+(5*4)+(4*4)+(3*1)+(2*5)+(1*9)=82
82 % 10 = 2
So 4441-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H21N/c11-9-5-4-8-10-6-2-1-3-7-10/h10H,1-9,11H2
4441-59-2Relevant academic research and scientific papers
Anodic benzylic C(sp3)-H amination: Unified access to pyrrolidines and piperidines
Herold, Sebastian,Bafaluy, Daniel,Mu?iz, Kilian
supporting information, p. 3191 - 3196 (2018/07/29)
An electrochemical aliphatic C-H amination strategy was developed to access the important heterocyclic motifs of pyrrolidines and piperidines within a uniform reaction protocol. The mechanism of this unprecedented C-H amination strategy involves anodic C-H activation to generate a benzylic cation, which is efficiently trapped by a nitrogen nucleophile. The applicability of the process is demonstrated for 40 examples comprising both 5- and 6-membered ring formations.
Interphenylene 7-Oxabicycloheptane Oxazoles. Highly Potent, Selective, and Long-Acting Thromboxane A2 Receptor Antagonists
Misra, Raj N.,Brown, Baerbel R.,Sher, Philip M.,Patel, Manorama M.,Hall, Steven E.,et al.
, p. 1401 - 1417 (2007/10/02)
A series of interphenylene 7-oxabicycloheptane oxazoles (2) were prepared and evaluated for their thromboxane (TxA2) antagonistic activity in vitro and duration of action in vivo.Examination of the carboxyl side chain indicated that the
