14707-75-6

Basic information

• Product Name: 1,3,5-TRIAZATRICYCLO[3.3.1.1(3,7)]DECAN-7-AMINE
• Synonyms: 1,3,5-TRIAZATRICYCLO[3.3.1.1(3,7)]DECAN-7-AMINE;TIMTEC-BB SBB001590;1,3,5-triazatricyclo[3.3.1.1~3,7~]decan-7-amine(SALTDATA: FREE);7-Amino-1,3,5-triazaadamantane
• CAS NO: 14707-75-6
• Molecular Formula: C₇H₁₄N₄
• Molecular Weight: 154.21
• Mol File: 14707-75-6.mol
• Article Data: 3

Chemical Properties

• Melting Point: 300-310 °C
• Boiling Point: 227.2±8.0 °C(Predicted)
• Appearance: /
• Density: 1.37±0.1 g/cm3(Predicted)
• PKA: 8.25±0.20(Predicted)
• CAS DataBase Reference: 1,3,5-TRIAZATRICYCLO[3.3.1.1(3,7)]DECAN-7-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-TRIAZATRICYCLO[3.3.1.1(3,7)]DECAN-7-AMINE(14707-75-6)
• EPA Substance Registry System: 1,3,5-TRIAZATRICYCLO[3.3.1.1(3,7)]DECAN-7-AMINE(14707-75-6)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 14707-75-6(Hazardous Substances Data)

Usage

General Description

1,3,5-Triazatricyclo[3.3.1.1(3,7)]decan-7-amine is a chemical compound that has a tricyclic structure with a nitrogen atom at the 7th position. It belongs to the class of amines, which are organic compounds containing a basic nitrogen atom. 1,3,5-TRIAZATRICYCLO[3.3.1.1(3,7)]DECAN-7-AMINE is a heterocyclic amine, meaning it has a ring structure with at least one non-carbon atom. The specific arrangement of nitrogen in the tricyclic structure gives this compound unique properties and reactivity. It may be used in various chemical reactions, pharmaceuticals, or other applications due to its specific structure and properties.

Upstream product

• 14612-28-3 7-nitro-1,3,5-triazaadamantane 

Downstream Products

• 52100-95-5 7-Chlor-1,3,5-triazaadamantan 
• 129058-65-7 N-bruneomycinyl-7-amino-1,3,5-triazaadamantane 

Relevant articles and documents

HETEROADAMANTANES AND THEIR DERIVATIVES. 4. SYNTHESIS OF 1,3,5-TRIAZAADAMANTANE

Reduction of 7-nitro-1,3,5-triazaadamantane with hydrazine hydrate in the presence of Raney nickel gave 7-hydroxyamino- and 7-amino-1,3,5-triazaadamantane, from which 7-chloro-, 7-bromo-, and 7-thiocyanato-1,3,5-triazaadamantanes were synthesized by substitutive deamination.Desulfurization of 7-thiocyanato-1,3,5-triazaadamantane in the presence of Raney nickel gave 1,3,5-triazaadamantane.

7-(N-Methyl-N-alkylamino)-1,3,5-triazaadamantanes

A series of high-density 7-(N-methyl-N-alkylamino)-1,3,5 triazaadamantanesre prepared. The preparation involves first adding the alkyl group to the parent amine by reacting the amine with a suitable aldehyde and hydrogen in the presence of a platinum catalyst and then reacting the thus produced secondary amine with formaldehyde and hydrogen in the presence of a nickel catalyst to produce the final product. The series represents a new class of fuels which is particularly useful in volume-limited applications.