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6601-22-5

6601-22-5 Structure

6601-22-5 Structure
IdentificationBack Directory
[Name]

2,4-DICHLORO-6-MORPHOLINO-1,3,5-TRIAZINE
[CAS]

6601-22-5
[Synonyms]

EOS-60795
AKOS 90019
4-DICHLORO-6-MORPHOLINO-1
2,4-Dichloro-6-Morpholino-1,3,
2,4-DICHLORO-6-MORPHOLINO-1,3,5-TRIAZINE
4-(4,6-dichloro-1,3,5-triazin-2-yl)morph
2,6-Dichloro-4-morpholino-1,3,5-triazine
2,4-Chloro-6-(morpholin-4-yl)-1,3,5-triazine
4-(4,6-dichloro-1,3,5-triazin-2-yl)morpholine
2,4-Dichloro-6-(morpholin-4-yl)-1,3,5-triazine
1,3,5-Triazine, 2,4-dichloro-6-(4-morpholinyl)-
[EINECS(EC#)]

229-544-9
[Molecular Formula]

C7H8Cl2N4O
[MDL Number]

MFCD00460178
[MOL File]

6601-22-5.mol
[Molecular Weight]

235.07
Chemical PropertiesBack Directory
[Melting point ]

137 °C
[Boiling point ]

441.9±55.0 °C(Predicted)
[density ]

1.503±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

powder to crystal
[pka]

1.01±0.10(Predicted)
[color ]

White to Almost white
[InChI]

InChI=1S/C7H8Cl2N4O/c8-5-10-6(9)12-7(11-5)13-1-3-14-4-2-13/h1-4H2
[InChIKey]

UQAMDAUJTXFNAD-UHFFFAOYSA-N
[SMILES]

N1=C(N2CCOCC2)N=C(Cl)N=C1Cl
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

22-37/38-41
[Safety Statements ]

26-39
[HS Code ]

2934.99.4400
Spectrum DetailBack Directory
[Spectrum Detail]

2,4-DICHLORO-6-MORPHOLINO-1,3,5-TRIAZINE(6601-22-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

Morpholine

110-91-8

2,4-DICHLORO-6-MORPHOLINO-1,3,5-TRIAZINE

6601-22-5

The general procedure for the synthesis of 2,4-dichloro-6-morpholino-1,3,5-triazine from morpholine was as follows: to a solution of cyanuric acid (230.5 g, 1,250 mmol) in acetone (2.25 L) was slowly added dropwise at 5°C morpholine (98.0 g, 1,125 mmol) and triethylamine (113.0 g, 1,125 mmol) in acetone (2.25 L) solution. After completion of the reaction, the resulting mixture was poured into water to precipitate the product. The white precipitate was collected by filtration and washed with methanol to give final white crystals 2,4-dichloro-6-morpholino-1,3,5-triazine (231.9 g, 986.9 mmol) in 88% yield. The mass spectrum (MS) of the product showed m/z: 234 (M+) and the nuclear magnetic resonance hydrogen spectrum (1H-NMR, CDCl3) showed δ: 3.75 (4H, triple peak, J=4Hz), 3.87 (4H, triple peak, J=4Hz).

[References]

[1] Patent: US2007/244110, 2007, A1. Location in patent: Page/Page column 4
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