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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)-

2-Quinazolinamine, 5-bromo-

Nc1ncc2c(n1)cccc2Br Request for Quotation
Chemical Name: 2-Quinazolinamine, 5-bromo-
CAS Number: 181871-83-0
Product Number: AG00236I(AGN-PC-09RXJG)
Synonyms:
MDL No:
Molecular Formula: C8H6BrN3
Molecular Weight: 224.0573

Identification/Properties

Computed Properties
Molecular Weight:
224.061g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
222.975g/mol
Monoisotopic Mass:
222.975g/mol
Topological Polar Surface Area:
51.8A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
164
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromoquinazolin-2-amine, a versatile chemical compound, finds key applications in chemical synthesis due to its unique properties and reactivity. This compound serves as a crucial building block in the production of various pharmaceuticals, agrochemicals, and materials. In organic synthesis, 5-Bromoquinazolin-2-amine acts as a valuable starting material for the construction of heterocyclic compounds, which are widely utilized in drug discovery and development. Its ability to undergo various functional group transformations makes it a valuable tool for synthesizing complex molecules with specific biological activities. Additionally, 5-Bromoquinazolin-2-amine plays a significant role in the development of novel chemical entities for research purposes, showcasing its importance in advancing the field of organic chemistry.