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212779-21-0

212779-21-0 Structure

212779-21-0 Structure
IdentificationBack Directory
[Name]

2-Amino-3-bromo-6-chloropyrazine
[CAS]

212779-21-0
[Synonyms]

104365
2-Amino-3-bromo-6-chL
3-Bromo-6-chloro-2-pyrazinamine
2-Amino-3-bromo-6-chloropyrazine
2-PyrazinaMine, 3-broMo-6-chloro-
3-Bromo-6-chloro-pyrazin-2-ylamine
2-Amino-3-bromo-6-chloropyrazine ISO 9001:2015 REACH
[Molecular Formula]

C4H3BrClN3
[MDL Number]

MFCD11044158
[MOL File]

212779-21-0.mol
[Molecular Weight]

208.446
Chemical PropertiesBack Directory
[Boiling point ]

299.5±35.0 °C(Predicted)
[density ]

1.960
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[pka]

0.05±0.10(Predicted)
[Appearance]

Off-white to light yellow Solid
[InChI]

InChI=1S/C4H3BrClN3/c5-3-4(7)9-2(6)1-8-3/h1H,(H2,7,9)
[InChIKey]

BOLCKGGORFPPJC-UHFFFAOYSA-N
[SMILES]

C1(N)=NC(Cl)=CN=C1Br
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H335-H319-H315
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P270-P301+P312-P330-P501-P264-P280-P302+P352-P321-P332+P313-P362
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

2-amino-3-bromo-6-chloropyrazine has essential applications in the pharmaceutical industry and is an important intermediate for synthesizing an anti-tumor medicament SHP2 inhibitor.
[Preparation]

Currently, in thepreparing 2-amino-3-bromo-6-chloropyrazine, the 2-amino-6-chloropyrazine is mainly obtained by a one-step bromination reaction. According to the method, bromine is mainly positioned at an amino para position due to the activation effect of amino; generated byproducts are mainly 2-bromo-3-chloro-5-aminopyrazine and partial dibromo byproduct 2-amino-3, 5-dibromo-6-chloropyrazine, the product 2-amino-3-bromo-6-chloro is less, the yield is low. A process for preparing 2-amino-3-bromo-6-chloropyrazine uses 3-aminopyrazine-2-carboxylate as raw material and includes such steps as chlorination, diazotization bromination, ester hydrolysis, carboxyl rearrangement and removing tert-butyloxycarbonyl.
Spectrum DetailBack Directory
[Spectrum Detail]

2-Amino-3-bromo-6-chloropyrazine(212779-21-0)1HNMR
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