860351-60-6 Usage
Description
(1S,3S)-cyclohexane-1,3-diamine, also known as trans-1,3-diaminocyclohexane, is a chiral chemical compound with the molecular formula C6H14N2. It features two stereocenters and exists in two enantiomeric forms, (1S,3S)and (1R,3R)-cyclohexane-1,3-diamine. (1S,3S)-cyclohexane-1,3-diamine is recognized for its versatile applications across various industries due to its unique structural and chemical properties.
Uses
Used in Asymmetric Catalysis:
(1S,3S)-cyclohexane-1,3-diamine serves as a crucial ligand in asymmetric catalysis, a technique that is pivotal in the synthesis of enantiomerically pure compounds. Its chiral nature allows for the selective formation of desired enantiomers, which is essential in producing biologically active molecules.
Used in Pharmaceutical and Agrochemical Synthesis:
As a building block, (1S,3S)-cyclohexane-1,3-diamine is utilized in the creation of various pharmaceuticals and agrochemicals. Its structural attributes make it a valuable component in the development of new drugs and agricultural chemicals, contributing to advancements in healthcare and agriculture.
Used in Coordination Chemistry:
(1S,3S)-cyclohexane-1,3-diamine functions as a chelating agent in coordination chemistry, enabling the formation of stable complexes with metal ions. This property is significant in the development of catalysts and materials with specific properties for various applications.
Used in Polymer and Resin Production:
(1S,3S)-cyclohexane-1,3-diamine is also employed in the production of polymers and resins, where its chemical properties contribute to the formation of materials with tailored characteristics for use in coatings, adhesives, and composites.
Used in Dye, Pigment, and Coating Industries:
(1S,3S)-cyclohexane-1,3-diamine finds application in the dye, pigment, and coating industries, where it is used to produce colorants and coatings with specific properties, such as improved stability and color intensity.
Used in the Development of Novel Materials:
Due to its unique structural and chemical properties, (1S,3S)-cyclohexane-1,3-diamine has potential applications in the development of novel materials, including those with enhanced performance characteristics for specialized uses.
Used in Drug Compound Development:
(1S,3S)-cyclohexane-1,3-diamine also holds promise in the development of new drug compounds, where its properties can be leveraged to create innovative therapeutic agents with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 860351-60-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,0,3,5 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 860351-60:
(8*8)+(7*6)+(6*0)+(5*3)+(4*5)+(3*1)+(2*6)+(1*0)=156
156 % 10 = 6
So 860351-60-6 is a valid CAS Registry Number.
860351-60-6Relevant articles and documents
Discovery of cyclopentane- and cyclohexane-trans-1,3-diamines as potent melanin-concentrating hormone receptor 1 antagonists
Giordanetto, Fabrizio,Karlsson, Olle,Lindberg, Jan,Larsson, Lars-Olof,Linusson, Anna,Evertsson, Emma,Morgan, David G.A.,Inghardt, Tord
, p. 4232 - 4241 (2007)
We herein report the optimization of cyclopentane- and cyclohexane-1,3-diamine derivatives as novel and potent MCH-R1 antagonists. Structural modifications of the 2-amino-quinoline and thiophene moieties found in the initial lead compound served to improve its metabolic stability profile and MCH-R1 affinity, and revealed unprecedented SAR when compared to other 2-amino-quinoline-containing MCH-R1 antagonists.
