ChemicalBook--->CAS DataBase List--->1120-99-6

1120-99-6

1120-99-6 Structure

1120-99-6 Structure
IdentificationMore
[Name]

3-AMINO-1,2,4-TRIAZINE
[CAS]

1120-99-6
[Synonyms]

1,2,4-TRIAZIN-3-AMINE
1,2,4-TRIAZIN-3-YLAMINE
3-AMINO-1,2,4-TRIAZINE
TIMTEC-BB SBB004379
3-amino-as-triazin
3-amino-as-triazine
1,2,4-Triazine-3-amine
[EINECS(EC#)]

214-324-7
[Molecular Formula]

C3H4N4
[MDL Number]

MFCD00006459
[Molecular Weight]

96.09
[MOL File]

1120-99-6.mol
Chemical PropertiesBack Directory
[Appearance]

BROWN CRYSTALLINE POWDER
[Melting point ]

174-177 °C(lit.)
[Boiling point ]

169.59°C (rough estimate)
[density ]

1.2170 (rough estimate)
[refractive index ]

1.7380 (estimate)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

DMSO (Sonicated), Methanol (Slightly, Sonicated)
[form ]

Crystalline Powder
[pka]

3.67±0.63(Predicted)
[color ]

Brown
[InChI]

InChI=1S/C3H4N4/c4-3-5-1-2-6-7-3/h1-2H,(H2,4,5,7)
[InChIKey]

MJIWQHRXSLOUJN-UHFFFAOYSA-N
[SMILES]

N1C=CN=C(N)N=1
[CAS DataBase Reference]

1120-99-6(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection .
[WGK Germany ]

3
[RTECS ]

XY2969000
[HS Code ]

29336990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Chemical Properties]

BROWN CRYSTALLINE POWDER
[Uses]

1,2,4-Triazin-3-amine can be used as integrade inhibiting antiviral agents.
[Synthesis]

1,2-Ethenediylbis(oxy) (9CI)

131543-46-9

Aminoguanidine bicarbonate

2582-30-1

3-AMINO-1,2,4-TRIAZINE

1120-99-6

Example 22 Synthesis of 1,2,4-triazin-3-amine (16): an aqueous solution of glyoxal (57 kg, 40 wt% aqueous, 393 mol, 0.73 eq.) was slowly added to a suspension of aminoguanidine bicarbonate (73 kg, 536.3 mol) in water (400 L) and the reaction was carried out at room temperature. Immediately after addition, the release of carbon dioxide (CO2) gas was observed. The reaction mixture was stirred continuously at room temperature for 18 hours, and the gas release essentially stopped after about 2 hours. Upon completion of the reaction, the mixture was separated by filtration and the filtrate was evaporated to dryness under reduced pressure. The resulting residue was extracted with cold methanol (MeOH, 3 x 120 L) and the combined methanol extracts were cooled to 0-5 °C to remove insoluble solids. Subsequently, the filtrate was concentrated under reduced pressure and the residue was recrystallized in acetonitrile to give the final 1,2,4-triazin-3-amine (16, 34 kg, theoretical yield 37.76 kg, 90% yield) as fine white needle-like crystals.

[References]

[1] Patent: US2009/291956, 2009, A1. Location in patent: Page/Page column 25-26
[2] Chemistry - A European Journal, 2015, vol. 21, # 41, p. 14376 - 14381
[3] Patent: WO2009/29625, 2009, A1. Location in patent: Page/Page column 75
Spectrum DetailBack Directory
[Spectrum Detail]

3-AMINO-1,2,4-TRIAZINE(1120-99-6)1HNMR
3-AMINO-1,2,4-TRIAZINE(1120-99-6)FT-IR
3-AMINO-1,2,4-TRIAZINE(1120-99-6)IR
3-AMINO-1,2,4-TRIAZINE(1120-99-6)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

3-Amino-1,2,4-triazine, 97%(1120-99-6)
[Sigma Aldrich]

1120-99-6(sigmaaldrich)
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