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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3-bromo-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine;hydrochloride

Brc1cnc2n1CCNC2 Request for Quotation
Chemical Name: 3-bromo-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine;hydrochloride
CAS Number: 954239-19-1
Product Number: AG00IJ35(AGN-PC-0712J4)
Synonyms:
MDL No:
Molecular Formula: C6H8BrN3
Molecular Weight: 202.0518

Identification/Properties

Computed Properties
Molecular Weight:
202.055g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
200.99g/mol
Monoisotopic Mass:
200.99g/mol
Topological Polar Surface Area:
29.8A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
130
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
3259
Hazard Statements:
H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Bromo-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine is a versatile compound used in chemical synthesis for various applications. In organic chemistry, it serves as a key building block for the construction of heterocyclic structures due to its unique molecular properties. This compound can participate in diverse reactions such as nucleophilic substitution, palladium-catalyzed cross-coupling, and cycloaddition reactions to generate complex organic molecules with potential pharmaceutical or industrial significance. Additionally, 3-Bromo-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine can be employed in the synthesis of bioactive compounds, agrochemicals, and materials science research, highlighting its importance as a valuable intermediate in the realm of chemical synthesis.