1598408-92-4

Basic information

• Product Name: (1R,2R)-N,N′-bis[thiophen-3-ylmethylidene]cyclohexane-1,2-diamine
• Synonyms: (1R,2R)-N,N′-bis[thiophen-3-ylmethylidene]cyclohexane-1,2-diamine
• CAS NO: 1598408-92-4
• Molecular Weight: 302.464
• Mol File: 1598408-92-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1R,2R)-N,N′-bis[thiophen-3-ylmethylidene]cyclohexane-1,2-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R)-N,N′-bis[thiophen-3-ylmethylidene]cyclohexane-1,2-diamine(1598408-92-4)
• EPA Substance Registry System: (1R,2R)-N,N′-bis[thiophen-3-ylmethylidene]cyclohexane-1,2-diamine(1598408-92-4)

Safety Data

• Hazardous Substances Data: 1598408-92-4(Hazardous Substances Data)

Upstream product

• 498-62-4 3-thiophene carboxaldehyde 
• 32044-22-7 (1R,2R)-1,2-diaminocyclohexane tartrate 

Downstream Products

• 1598408-96-8 (1R,2R)-N,N′-bis(thiophen-3-ylmethyl)cyclohexane-1,2-diamine 

Relevant articles and documents

Synthesis and fluorescent properties of novel chiral 1,2-diaminocyclohexane substituted ligands and their complexes

A series of novel chiral 1,2-diaminocyclohexane derivatives bearing heterocyclic units were synthesized via improved methods under ultrasonic irradiation. The photophysical properties of compounds were studied in ethanol, methanol, and chloroform. The sensitivity of these amines toward Cu 2+, Cd2+, and Ni2+ was studied by the UV-vis and fluorescent methods. The π-electron structure of thiophene and bithiophene containing sensors is the most active toward all above mentioned metal ions and is highly selective for Ni2+ and Cd2+.