389623-48-7

Basic information

• Product Name: 2H-Pyrimido[1,2-a]pyrimidine,octahydro-(9CI)
• Synonyms: 2H-Pyrimido[1,2-a]pyrimidine,octahydro-(9CI)
• CAS NO: 389623-48-7
• Molecular Formula: C7H15N3
• Molecular Weight: 0
• Product Categories: AMINETERTIARY
• Mol File: 389623-48-7.mol
• Article Data: 16

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2H-Pyrimido[1,2-a]pyrimidine,octahydro-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyrimido[1,2-a]pyrimidine,octahydro-(9CI)(389623-48-7)
• EPA Substance Registry System: 2H-Pyrimido[1,2-a]pyrimidine,octahydro-(9CI)(389623-48-7)

Safety Data

• Hazardous Substances Data: 389623-48-7(Hazardous Substances Data)

Upstream product

• 56-18-8 bis(3-aminopropyl)amine 
• 726-42-1 di-p-tolylcarbodiimide 
• 74569-03-2 Bis(3-aminopropyl)amin-trihydrobromid 
• 74569-04-3 3,4,6,7,8,9-Hexahydro-2H-pyrimido<1,2-a>pyrimidin-hydrobromid 
• 113-00-8 guanidine nitrate 
• 616-38-6 carbonic acid dimethyl ester 
• 13173-07-4 1-(3-aminopropyl)tetrahydro-2(1H)-pyrimidinone 
• 124-38-9 carbon dioxide 
• 1333123-47-9 C₇H₁₃N₃*C₁₆H₁₄O₃ 
• 1333123-53-7 C₁₅H₁₀O₄*C₇H₁₃N₃ 
• 538-75-0 dicyclohexyl-carbodiimide 
• 693-13-0 diisopropyl-carbodiimide 
• 50-01-1 guanidine hydrochloride 
• 420-04-2 CYANAMID 

Downstream Products

• 1333123-47-9 C₇H₁₃N₃*C₁₆H₁₄O₃ 
• 84030-20-6 1-methyl-2,3,4,6,7,8-hexahydro-1H-pyrimido[1,2-a]pyrimidine 
• 107-31-3 Methyl formate 
• 1356453-15-0 CH₂O₂*C₇H₁₃N₃ 
• 1587726-62-2 7-(4-Methyl-1H-imidazol-1-yl)-2-[(1S)-1-{(2S,5R)-5-[4-(trifluoromethyl)phenyl]tetrahydrofuran-2-yl}ethyl]-3,4-di hydro-2H-pyrido[1,2-a]pyrazine-1,6-dione 
• 1430747-09-3 C₁₃H₂₇N₄P*C₇H₈O₃S 
• 62051-24-5 hexahydro-3a,6a,9a-triaza-9b-phospha-phenalene 
• 1366629-58-4 (1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidineH)[SbCl3(1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine(-1H))2] 

Relevant articles and documents

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Super alkali material and preparation method thereof, and organic light-emitting diode

The invention discloses a super alkali material and a preparation method thereof, and an organic light-emitting diode. The super alkali material has a general structural formula as described in the specification. In the general structural formula, aromatic rings Ar1, Ar2, Ar3 and Ar4 are respectively and independently selected from substituted or unsubstituted aryl or heteroaryl groups; N is a nitrogen atom; E is the same or different, and each E is an sp2-hybridized carbon or nitrogen atom; and Cy1, Cy2, Cy3 and Cy4 are respectively and independently selected from substituted or unsubstituted heterocyclic rings. The electron injection performance of a device can be effectively improved by introducing a functional group with an alkaline acid dissociation constant (pKa), and a planar rigid structure is adopted, so the material is closely stacked to show high electron mobility, the glass-transition temperature (Tg) of the material is increased, and the stability of the device is improved. On the premise that HOMO and LUMO energy levels are maintained, injection energy barriers are reduced, turn-on voltage is reduced, and when the material serves as an electron transport material of the organic light-emitting diode, the material has the advantages of being high in carrier mobility, excellent in device performance, good in stability and the like.

PROCESS FOR PREPARING BICYCLIC GUANIDINES

Bicyclic guanidines are prepared by reacting dialkylenetriamines with dialkylcarbonates in the presence of a silane of the formula [in-line-formulae]Si(ORx)oRY(4?o) ??(IV)[/in-line-formulae] and/or their partial hydrolysates, with the proviso that contain minimally one unit IV which is a monovalent optionally substituted hydrocarbon radial with 3 to 10 carbon atoms.

METHOD FOR PREPARING A BICYCLIC GUANIDINE AND ITS DERIVATIVES

The present invention relates to a method of producing a bicyclic guanidine and its derivatives. In particular, the present invention relates to a method of producing triazabicyclodecene (TBD) and its derivatives, particularly alkyl derivatives, such as methyl triazabicyclodecene (MTBD), and MTBD-derived ionic liquids. The invention also relates to the use of said compounds in cellulose dissolution and subsequent processing.