10029-07-9

Usage

Uses

Used in Chemical Synthesis:
[4-(aminomethyl)cyclohexyl]methanamine is used as a chemical intermediate for the synthesis of various compounds. Its reactivity, stemming from the amine groups, makes it a valuable building block in the creation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [4-(aminomethyl)cyclohexyl]methanamine is used as a precursor in the development of new drugs. Its ability to form a wide range of chemical bonds allows it to be incorporated into the structures of potential therapeutic agents.
Used in Material Science:
[4-(aminomethyl)cyclohexyl]methanamine is used as a component in the formulation of advanced materials. Its presence can influence the properties of materials, such as their reactivity, solubility, or stability, making it a useful additive in material science applications.
Used in Research and Development:
In research and development settings, [4-(aminomethyl)cyclohexyl]methanamine is used as a model compound for studying the properties and reactions of amines. Its unique structure provides insights into the behavior of similar compounds and can aid in the discovery of new chemical reactions and processes.

InChI:InChI=1/C8H18N2/c9-5-7-1-2-8(6-10)4-3-7/h7-8H,1-6,9-10H2

Upstream product

• 27687-14-5 trans 4-(tert-butyloxycarbonylamino)methylcyclohexanecarboxylic acid 
• 619-82-9 trans-hexahydroterephthalic acid 
• 619-81-8 cis-cyclohexane-1,4-dicarboxylic acid 
• 6550-85-2 trans-1,4-cyclohexanedicarbonitrile 
• 54657-09-9 trans-1,4-di(carboxamido)cyclohexane 
• 70925-16-5 cis-cyclohexane-dicarboxylic acid-(1.4)-diamide 
• 13170-66-6 trans-1,4-cyclohexanedicarboxylic acid dichloride 
• 57702-84-8 trans-1,4-Bis(bromomethyl)cyclohexane 
• 10534-13-1 cyclohexane-1,4-dicarbonitrile 
• 619-81-8 cyclohexane-1,4-dicarboxylic acid 
• 100-21-0 terephthalic acid 
• 2549-93-1 1,4-bis-(aminomethyl)cyclohexane 
• 14571-47-2 (1s,4s)-cyclohexane-1,4-dicarbonyl dichloride 
• 749866-15-7 trans-4-[[(tert-butoxycarbonyl)amino]methyl]cyclohexanecarboxylic acid amide 

Downstream Products

• 55778-73-9 N,N'-(trans-1,4-cyclohexylenebismethyl)-bis[2-hydroxydecylamine] 
• 28282-15-7 C₂₄H₂₄F₆N₂O₄ 
• 28282-17-9 C₂₄H₃₀N₂O₄ 
• 35873-55-3 N,N'-trans-cyclohexane-1,4-diyldimethyl-bis-carbamic acid bis-(2-chloro-ethyl) ester 
• 1174-29-4 N.N'-Di--cyclohexan-trans-1.4-bis-methylamin 
• 1170-78-1 N_.N'-Dicyclooctyl-cyclohexan-trans-1.4-bis-methylamin 
• 1246-07-7 N_.N'-Diheptanoyl-cyclohexan-trans-1.4-bis-methylamin 
• 1170-59-8 N.N'-Di--cyclohexan-trans-1.4-bis-methylamin 
• 1166-44-5 N_.N'-Dicyclopentanoyl-cyclohexan-trans-1.4-bis-methylamin 
• 3056-82-4 N_.N'-Dibenzyl-cyclohexan-trans-1.4-bis-methylamin 
• 3056-85-7 N.N'-Di-<2-fluor-benzyl>-cyclohexan-trans-1.4-bis-methylamin 
• 1227-59-4 N_.N'-Dibutyryl-cyclohexan-trans-1.4-bis-methylamin 
• 1166-41-2 N_.N'-Di-(2-hydroxy-cyclohexyl)-cyclohexan-trans-1.4-bis-methylamin 
• 1241-22-1 N.N'-Di-<3-methyl-cyclohexyl>-cyclohexan-trans-1.4-bis-methylamin 

Relevant academic research and scientific papers

PRODUCTION METHOD FOR 1,4-CYCLOHEXANEDICARBOXYLIC ACID DERIVATIVE, 1,4-DICYANOCYCLOHEXANE AND 1,4-BIS(AMINOMETHYL)CYCLOHEXANE

A production method for producing a 1,4-cyclohexanedicarboxylic acid derivative, involves subjecting an aqueous ammonia solution of 1,4-cyclohexanedicarboxylic acid to heat concentration, thereby precipitating a 1,4-cyclohexanedicarboxylic acid derivative as a crystal.

1,4-BIS(ISOCYANATOMETHYL)CYCLOHEXANE, POLYISOCYANATE COMPOSITION, POLYURETHANE RESIN, MOLDED ARTICLE, FIBER, FABRIC, NONWOVEN, FILM, SHEET AND APPAREL

1,4-bis(isocyanatomethyl)cyclohexane contains 70 mol% or more and 95 mol% or less of a trans isomer relative to a total amount of a cis isomer and the trans isomer, and 0.1 ppm or more and 300 ppm or less of the compound represented by formula (1) below:

METHOD FOR PRODUCING TRANS-BIS(AMINOMETHYL)CYCLOHEXANE, METHOD FOR PRODUCING BIS(ISOCYANATOMETHYL)CYCLOHEXANE, BIS(ISOCYANATOMETHYL)CYCLOHEXANE, POLYISOCYANATE COMPOSITION, AND POLYURETHANE RESIN

A method for producing trans-bis(aminomethyl)cyclohexane includes a trans-isomerization step in which cis-dicyanocyclohexane is isomerized into trans-dicyanocyclohexane by heating dicyanocyclohexane containing cis-dicyanocyclohexane in the presence of a t

METHOD FOR PRODUCING TRANS-1,4-BIS(AMINOMETHYL)CYCLOHEXANE

A method for producing trans-1,4-bis(aminomethyl)cyclohexane includes a nuclear hydrogenation step of producing a hydrogenated terephthalic acid or terephthalic acid derivative by nuclear hydrogenation of a terephthalic acid or terephthalic acid derivative, the terephthalic acid or terephthalic acid derivative being at least one selected from the group consisting of terephthalic acid, terephthalic acid ester, and terephthalic acid amide; a cyanation step of treating the hydrogenated terephthalic acid or terephthalic acid derivative with ammonia, thereby producing 1,4-dicyanocyclohexane, and producing trans-1,4-dicyanocyclohexane from the obtained 1,4-dicyanocyclohexane; and an aminomethylation step of treating the trays-1,4-dicyanocyclohexane with hydrogen, thereby producing trans-1,4-bis(aminomethyl)cyclohexane. Metal oxide is used as a catalyst in the cyanation step, and the obtained trans-1,4-dicyanocyclohexane has a metal content of 3000 ppm or less.

Preparation of Fluorescent Nonpeptidic Neuropeptide Y Receptor Ligands: Analogues of the Quinazoline-type Anti-obesity Y5 Antagonist CGP 71683A

As part of a programme to develop fluorescence-based methods for the study of the interactions between G-protein coupled receptors (GPCRs) and their ligands the preparation of low molecular weight fluorescence-labelled neuropeptide Y (NPY) Y5 a