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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-Bromoquinolin-5-amine

Brc1cnc2c(c1)c(N)ccc2 Request for Quotation
Chemical Name: 3-Bromoquinolin-5-amine
CAS Number: 116632-57-6
Product Number: AG000CWZ(AGN-PC-0WAIFB)
Synonyms:
MDL No:
Molecular Formula: C9H7BrN2
Molecular Weight: 223.0693

Identification/Properties

Computed Properties
Molecular Weight:
223.073g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
221.979g/mol
Monoisotopic Mass:
221.979g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
163
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-H315-H320-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Bromoquinolin-5-amine, also known as $name$, is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. This specific molecule plays a crucial role in various chemical reactions and organic transformations, making it an essential building block in the synthesis of pharmaceuticals, agrochemicals, and materials.One of the key applications of 3-Bromoquinolin-5-amine is its use as a key intermediate in the preparation of heterocyclic compounds such as quinoline derivatives. These compounds are important in medicinal chemistry as they exhibit a wide range of biological activities, including anti-cancer, anti-inflammatory, and antimicrobial properties. By incorporating 3-Bromoquinolin-5-amine into the synthesis of these compounds, researchers can efficiently access diverse chemical structures with potential therapeutic benefits.Furthermore, 3-Bromoquinolin-5-amine can serve as a valuable starting material for constructing complex molecules through various functionalization reactions. Its unique bromoquinoline scaffold offers strategic sites for further modification, enabling chemists to introduce different functional groups or structural motifs to tailor the properties of the final compound. This versatility makes 3-Bromoquinolin-5-amine a valuable tool for designing and synthesizing novel molecules with desired properties for specific applications.Overall, the importance of 3-Bromoquinolin-5-amine in chemical synthesis lies in its ability to facilitate the creation of diverse compounds with potential pharmaceutical, agricultural, or materials applications. Its role as a versatile building block underscores its significance in modern organic chemistry and underscores its value in advancing scientific research and innovation.