31121-12-7

Usage

Uses

Used in Pharmaceutical Industry:
3-(cyclohexylamino)propan-1-ol is used as a building block for the synthesis of various pharmaceuticals, due to its ability to form stable amide and imine linkages with other molecules, enhancing the drug's efficacy and stability.
Used in Agrochemical Industry:
3-(cyclohexylamino)propan-1-ol is used as a building block for the synthesis of various agrochemicals, contributing to the development of effective and stable pesticides and herbicides.
Used as a Corrosion Inhibitor:
3-(cyclohexylamino)propan-1-ol is used as a corrosion inhibitor in various industrial applications, such as in the oil and gas industry, to protect metal surfaces from corrosion and extend the life of equipment.
Used in Rubber Chemical Production:
3-(cyclohexylamino)propan-1-ol is used as an intermediate in the production of rubber chemicals, contributing to the development of high-quality rubber products with improved properties.
Used in Antioxidant Production:
3-(cyclohexylamino)propan-1-ol is used as an intermediate in the production of antioxidants, which are essential in various industries to prevent the oxidation and degradation of materials, thereby extending their shelf life and performance.

InChI:InChI=1/C9H19NO/c11-8-4-7-10-9-5-2-1-3-6-9/h9-11H,1-8H2

Upstream product

• 108-91-8 cyclohexylamine 
• 627-18-9 1-bromo-3-propanol 
• 99976-68-8 1-(3-hydroxy-propylamino)-cyclohexanecarbonitrile 
• 627-30-5 1-chloro-3-hydroxypropane 
• 22870-26-4 methyl 3-cyclohexylaminopropionate 
• 108-94-1 cyclohexanone 

Downstream Products

• 128218-33-7 2-cyclohexylisothiazolidine 1-oxide 
• 105695-32-7 N-Cyclohexyl-N-(3-hydroxy-propyl)-4-(2-oxo-1,2,3,5-tetrahydro-imidazo[2,1-b]quinazolin-7-yloxy)-butyramide 
• 3592-79-8 3-(N-cyclohexylamino)propanethiol 
• 101866-88-0 cyclohexyl-(3-hydroxy-propyl)-carbamic acid benzyl ester 

Relevant academic research and scientific papers

Synthesis of Different Classes of Six-Membered Gold(I) NHC Complexes by the Isonitrile Route

Different types of six-membered N-heterocyclic gold carbene complexes were prepared by using gold(I) isonitrile complexes as precursors in combination with suitably functionalized amines. The simple procedures provide an easy access to not only unsymmetrically substituted saturated carbene complexes but rarely reported types of carbene complexes such as six-membered N-heterocyclic oxo-carbene complexes, and six-membered partly unsaturated ligands can be obtained following the strategy.

Templated assembly of medium cyclic ethers: Via exo-trig nucleophilic cyclization of cyclopropenes

A novel method for the assembly of medium heterocycles via an intramolecular nucleophilic addition to cyclopropenes generated in situ from the corresponding bromocyclopropanes is described. The exo-trig nucleophilic cyclizations were shown to proceed very

Diastereoselectivity control in formal nucleophilic substitution of bromocyclopropanes with oxygen- and sulfur-based nucleophiles

A diastereoconvergent formal nucleophilic substitution of bromocyclopropanes with oxygen- and sulfur-based nucleophiles is described. The reaction proceeds via in situ formation of a highly reactive cyclopropene intermediate and subsequent diastereoselect

Indirect monoalkylation of primary and secondary amines by reductive decyanation of α-aminonitriles with sodium cyanoborohydride-mercury bis(trifluoroacetate)

Secondary and tertiary amines are prepared from α-aminonitriles by selective reductive cleavage of the cyanide moiety. The α-aminonitriles in this case, function as 'masked' imine or iminium ions and are 'unmasked' by mercury(II) in the presence of sodium cyanoborohydride to obtain the reduced product. Secondary amines may be prepared indirectly from primary amines in good yield without danger of over alkylation.

SIMPLE SYNTHESIS OF 3-(N-ALKYLAMINO)-1-PROPANOLS

Various 3-(N-alkylamino)-1-propanols were obtained by the lithium aluminum hydride reduction of the products of the reaction of 3-amino-1-propanol with carbonyl compounds.This method for the synthesis of aminopropanols is applicable in the case of optimal electrophilicity of the carbonyl component.

Synthesis and Kinetics of the Formation of N-Substituted Cyclic Sulfinamides from Secondary Amine Disulfides

N-substituted cyclic saturated sulfinamides were prepared from two secondary amine disulfides, 3-propyl disulfide and 3-(cyclohexylamino)propyl disulfide, and two bicyclic sulfinamides were made from 2-(2-piperidyl)ethyl disulfide an