26150-46-9

Basic information

• Product Name: (1S,3S,5S)-CYCLOHEXANE-1,3,5-TRIAMINE
• Synonyms: (1S,3S,5S)-CYCLOHEXANE-1,3,5-TRIAMINE
• CAS NO: 26150-46-9
• Molecular Formula: C₆H₁₅N₃
• Molecular Weight: 129.2
• Mol File: 26150-46-9.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (1S,3S,5S)-CYCLOHEXANE-1,3,5-TRIAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,3S,5S)-CYCLOHEXANE-1,3,5-TRIAMINE(26150-46-9)
• EPA Substance Registry System: (1S,3S,5S)-CYCLOHEXANE-1,3,5-TRIAMINE(26150-46-9)

Safety Data

• Hazardous Substances Data: 26150-46-9(Hazardous Substances Data)

Upstream product

• 31044-90-3 cis-1,3,5-Triazidocyclohexane 
• 64-17-5 ethanol 
• 98096-07-2 1,3,5-tris(hydroxyamino)benzene 
• 50409-12-6 cis,cis-1,3,5-trihydroxycyclohexane 
• 31044-88-9 cis-1,3,5-Tris(phenylsulfonyloxy)cyclohexane 
• 177660-39-8 (3,5-Bis-benzyloxycarbonylamino-cyclohexyl)-carbamic acid benzyl ester 
• 621-22-7 (1Z)-cyclohexane-1,3,5-trione trioxime 

Downstream Products

• 118924-48-4 1r,3c,5c-tris-[2]pyridylmethylenamino-cyclohexane 
• 479251-80-4 N-trityl-cis,cis-1,3,5-triaminocyclohexane 
• 479251-79-1 N,N'-bis-trityl-cis,cis-1,3,5-triaminocyclohexane 
• 636-70-4 triethylamine hydrobromide 
• 758695-00-0 [[Ag(cis,cis-1,3,5-triaminocyclohexane)](tetrafluoroborate)].infin. 
• 1260177-89-6 cis,cis-1,3,5-tris(2,3,4,5,6-pentafluorobenzylideneamino)-cyclohexane 
• 1260177-90-9 cis,cis-1,3,5-tris(3,5-bis(trifluoromethyl)-benzylideneamino)cyclohexane 
• 1260177-87-4 cis,cis-1,3,5-tris(2,3,4,5,6-pentamethylbenzylideneamino)-cyclohexane 
• 1260177-91-0 cis,cis-1,3,5-tris(2-(trifluoromethyl)benzylideneamino)cyclohexane 
• 175673-38-8 cis,cis-1,3,5-tris(benzylideneamino)cyclohexane 
• 1260177-92-1 cis,cis-1,3,5-tris(2-methoxybenzylideneamino)-cyclohexane 
• 1260177-88-5 cis,cis-1,3,5-tris(2,6-dimethoxybenzylideneamino)-cyclohexane 

Relevant articles and documents

Analysis of the Proton, Carbon, and Nitrogen NMR Spectra of cis,cis- and cis,trans-1,3,5-Triaminocyclohexane

The proton spectrum of the isomeric mixture of cis,cis- and cis,trans-1,3,5-triaminocyclohexane was assigned with a 2D COSY experiment.Using Forrest's modified equation and the 2D J spectrum results, the conformations of the two isomers were analysed.The six-membered ring of the cis,trans isomer is flattened by 1,3-diaxial interactions between two amino substituents; in the cis,cis isomer, ring pucker is increased owing to non-bonded interaction between the equatorial amino groups and adjacent methylene protons.The 13C and 15N spin-lattice relaxation of the two isomeric 1,3,5-triaminocyclohexanes was also measured at different pH values; NHx groups rotate faster with decreasing pH.Rotation/jump rates and barriers are reported, determined from the NT1DD ratios between 15N and 13C nuclei.

A branched, hydrogen-bonded heterodimer: a novel system for achieving high stability and specificity

Presented is a description of the design, synthesis, and characterization of a novel, branched, six hydrogen-bonded heterodimer termed 'trident'. Two branched oligoamide molecules, 1 and 2, with complementary hydrogen-bonding sequences 3(AD) and 3(DA), re

Lipophilic Hexadentate Gallium, Indium and Iron Complexes of New Phenolate-derivatized Cyclohexanetriamines as Potential in vivo Metal-transfer Reagents

1,3,5-Tris(5-substituted salicylamino)cyclohexanes (H3L; R = H, NO2 or OMe) have been synthesized by Schiff-base condensation between cis-1,3,5-triaminocyclohexane and a substituted salicylaldehyde, followed by reduction with KBH4.Reaction of these compou