ChemicalBook--->CAS DataBase List--->89123-58-0

89123-58-0

89123-58-0 Structure

89123-58-0 Structure
IdentificationBack Directory
[Name]

5-BROMO-PYRAZINE-2,3-DIAMINE
[CAS]

89123-58-0
[Synonyms]

5-BROMO-2,3-DIAMINOPYRAZINE
5-BROMO-PYRAZINE-2,3-DIAMINE
2,3-Pyrazinediamine, 5-bromo-
Pyrazine, 2,3-diamino-5-bromo-
2,3-DIAMINO-5-BROMOPYRAZINE, 97%
5-BROMO-PYRAZINE-2,3-DIAMINE ISO 9001:2015 REACH
[Molecular Formula]

C4H5BrN4
[MDL Number]

MFCD06245575
[MOL File]

89123-58-0.mol
[Molecular Weight]

189.01
Chemical PropertiesBack Directory
[Melting point ]

212-216 °C (dec.)
[Boiling point ]

357.1±37.0 °C(Predicted)
[density ]

1.956±0.06 g/cm3(Predicted)
[storage temp. ]

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

solid
[pka]

2.72±0.10(Predicted)
[color ]

light brown
[InChI]

1S/C4H5BrN4/c5-2-1-8-3(6)4(7)9-2/h1H,(H2,6,8)(H2,7,9)
[InChIKey]

CPYAUFLEMLTQAA-UHFFFAOYSA-N
[SMILES]

Nc1ncc(Br)nc1N
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H317-H319-H335
[Precautionary statements ]

P280-P301+P312+P330-P302+P352-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22-36/37/38-43
[Safety Statements ]

26-36/37
[WGK Germany ]

3
[HS Code ]

2933998090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
Skin Sens. 1
STOT SE 3
Hazard InformationBack Directory
[Uses]

2,3-Diamino-5-bromopyrazine
[Synthesis]

2-Amino-3,5-dibromopyrazine

24241-18-7

5-BROMO-PYRAZINE-2,3-DIAMINE

89123-58-0

The general procedure for the synthesis of 5-bromo-2,3-diaminopyrazine from 2-amino-3,5-dibromopyrazine was as follows: step 1: 2-amino-3,5-dibromopyrazine (3 g, 11.64 mmol) was suspended in a 25% aqueous ammonia solution (15 mL) in a sealed tube and the reaction was heated for 16 h at 110 °C. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was partitioned between ethyl acetate and water (3 x 50 mL). The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography with 15% ethyl acetate-hexane mixed solvent as eluent to afford 5-bromo-2,3-diaminopyrazine as a yellow solid (2.1 g, 93% yield). Mass spectrum (electrospray ionization) m/z: 189 ([M+H]+).

[References]

[1] Patent: US2011/59118, 2011, A1. Location in patent: Page/Page column 81-82
[2] Bioorganic and Medicinal Chemistry, 1999, vol. 7, # 6, p. 1059 - 1065
[3] Patent: WO2017/64068, 2017, A1. Location in patent: Page/Page column 59; 60
[4] Patent: TWI523856, 2016, B. Location in patent: Paragraph 0078
[5] Patent: CN108395436, 2018, A. Location in patent: Paragraph 0010
Spectrum DetailBack Directory
[Spectrum Detail]

5-BROMO-PYRAZINE-2,3-DIAMINE(89123-58-0)1HNMR
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