ChemicalBook--->CAS DataBase List--->13134-38-8

13134-38-8

13134-38-8 Structure

13134-38-8 Structure
IdentificationBack Directory
[Name]

(PyrazinaMine, 3,6- diMethyl
[CAS]

13134-38-8
[Synonyms]

3,6-Dimethylpyrazinamine
(PyraziMine, 3,6- diMethyl
3,6-DiMethyl-2-pyrazinaMine
3,6-DIMETHYLPYRAZIN-2-AMINE
(PyrazinaMine, 3,6- diMethyl
2-Amino-3,6-dimethylpyrazine
3-Amino-2,5-dimethylpyrazine
2-PYRAZINAMINE, 3,6-DIMETHYL-
2-Amino-3,6-dimethylpyrazine 96%
2-Amino-3,6-dimethylpyrazine 3,6-Dimethylpyrazin-2-amine
[Molecular Formula]

C6H9N3
[MDL Number]

MFCD18917551
[MOL File]

13134-38-8.mol
[Molecular Weight]

123.16
Chemical PropertiesBack Directory
[Melting point ]

111-113℃ (benzene )
[Boiling point ]

119℃ (10 Torr)
[density ]

1.112±0.06 g/cm3 (20 ºC 760 Torr)
[Fp ]

124.5±13.1℃
[storage temp. ]

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

solid
[pka]

3.85±0.10(Predicted)
[Appearance]

Light yellow to brown Solid
[InChI]

InChI=1S/C6H9N3/c1-4-3-8-5(2)6(7)9-4/h3H,1-2H3,(H2,7,9)
[InChIKey]

HYZYHVUIWRRMEZ-UHFFFAOYSA-N
[SMILES]

C1(N)=NC(C)=CN=C1C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

3
[HS Code ]

2933998090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Spectrum DetailBack Directory
[Spectrum Detail]

(PyrazinaMine, 3,6- diMethyl(13134-38-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-CHLORO-2,5-DIMETHYLPYRAZINE

95-89-6

(PyrazinaMine, 3,6- diMethyl

13134-38-8

a. In a 100 mL autoclave, 3-chloro-2,5-dimethylpyrazine (25.0 g, 176 mmol), 25-28% w/w ammonia solution (80 mL), and copper powder (1.69 g, 26.4 mmol) were added sequentially. After sealing the autoclave, the mixture was heated to 150 °C and reacted under vigorous stirring for 48 hours. After completion of the reaction, the mixture was cooled to room temperature and concentrated under reduced pressure. The residue was diluted with brine (100 mL) and subsequently extracted with ethyl acetate (4 x 100 mL). The organic phases were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was washed with petroleum ether to give 2-amino-3,6-dimethylpyrazine (17.6 g, 81% yield) as a light yellow solid. eSI MS: m/z 124 [M + H]+.

[References]

[1] Patent: US2012/178748, 2012, A1. Location in patent: Page/Page column 37
[2] Patent: WO2015/177688, 2015, A1. Location in patent: Page/Page column 20
[3] Synthesis, 1994, # 9, p. 931 - 934
[4] Patent: WO2013/160419, 2013, A1. Location in patent: Page/Page column 33
[5] Patent: US2015/65507, 2015, A1. Location in patent: Paragraph 0169; 0170
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