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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-amino-6-bromopyrazin-2-yl)methanol

OCc1nc(Br)cnc1N Request for Quotation
Chemical Name: (3-amino-6-bromopyrazin-2-yl)methanol
CAS Number: 1260880-59-8
Product Number: AG000RI8(AGN-PC-0JF3TG)
Synonyms:
MDL No:
Molecular Formula: C5H6BrN3O
Molecular Weight: 204.0246

Identification/Properties

Computed Properties
Molecular Weight:
204.027g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
202.969g/mol
Monoisotopic Mass:
202.969g/mol
Topological Polar Surface Area:
72A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
113
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:
Warning
UN#:
N/A
Hazard Statements:
H302-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(3-Amino-6-bromopyrazin-2-yl)methanol is a versatile compound commonly used in chemical synthesis due to its unique properties and reactivity. This compound acts as a valuable building block in organic chemistry, serving as a key intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals.Its role in chemical synthesis includes serving as a precursor for the synthesis of heterocyclic compounds, which are essential in drug discovery and development. (3-Amino-6-bromopyrazin-2-yl)methanol can be further functionalized to introduce specific functional groups or pharmacophores, allowing chemists to tailor the structure of the final compound for desired biological activity.In addition, the presence of both an amino group and a bromine atom in the molecule provides synthetic chemists with convenient handles for further modifications through traditional organic reactions like nucleophilic substitution, acylation, and cross-coupling reactions. This enables the creation of complex molecules with intricate structures and diverse functionalities.Overall, the application of (3-Amino-6-bromopyrazin-2-yl)methanol in chemical synthesis showcases its importance as a crucial building block for the construction of biologically active compounds, making it a valuable tool in the field of medicinal and synthetic chemistry.