Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

494364

Sigma-Aldrich

2-Amino-3,5-dibromopyrazine

97%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C4H3Br2N3
CAS Number:
Molecular Weight:
252.89
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

assay

97%

mp

114-117 °C (lit.)

functional group

bromo

SMILES string

Nc1ncc(Br)nc1Br

InChI

1S/C4H3Br2N3/c5-2-1-8-4(7)3(6)9-2/h1H,(H2,7,8)

InChI key

DTLBKXRFWUERQN-UHFFFAOYSA-N

General description

2-Amino-3,5-dibromopyrazine can be synthesized from 2-aminopyrazine via bromination using N-bromosuccinimide (NBS). It reacts with sodium dicyanocuprate to form a mixture of mono and dicyanation products.[1] The formation of 2-aminothiazolopyrazines by reacting 2-amino-3,5-dibromopyrazine with isothiocyanates has been reported.[2]

Application

2-Amino-3,5-dibromopyrazine may be used in the synthesis of:
  • 2-amino-5-bromopyrazin-3-thiol[3]
  • 2-amino-3,5-bis(p-methoxyphenyl)-1,4-pyrazine[4]
  • 3,7-dihydroimidazo[1,2a]pyrazine-3-ones[5]

pictograms

Skull and crossbonesCorrosion

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Studies on pyrazines. XX, A simple synthesis of 5-substituted 2-amino-3-cyanopyrazines: useful intermediates for pteridine synthesis.
Synthesis 8 (1990): 659-660.
Sato N and Takeuchi R.
Synthesis, 8, 659-660 (1990)
Synthesis of Tetraaza Derivatives of Benzoxazinophenothiazine.
Ezema BE, et al.
Orient. J. Chem., 31(1), 133-139 (2015)
Synthesis of N-Substituted-2-Aminothiazolo [4,5-b] pyrazines by Tandem Reaction of o-Aminohalopyrazines with Isothiocyanates.
Kwak SH, et al.
Bull. Korean Chem. Soc., 33, 4271-4274 (2012)
Synthesis of 3,7-dihydroimidazo[1,2a]pyrazine-3-ones and their chemiluminescent properties.
Adamczyk M, et al.
Tetrahedron, 59(41), 8129-8142 (2003)
2,6-Diamino-3,5-diaryl-1,4-pyrazine derivatives as novel antioxidants.
Rees JF and Marchand-Brynaert J
Synthesis, 5, 768-772 (2001)

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service