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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)-

Phenol, 4-(3-aminopropyl)-, hydrobromide

NCCCc1ccc(cc1)O.Br Request for Quotation
Chemical Name: Phenol, 4-(3-aminopropyl)-, hydrobromide
CAS Number: 583825-30-3
Product Number: AG00VTH6(AGN-PC-00ACDK)
Synonyms:
MDL No:
Molecular Formula: C9H14BrNO
Molecular Weight: 232.1176

Identification/Properties

Computed Properties
Molecular Weight:
232.121g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
231.026g/mol
Monoisotopic Mass:
231.026g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
97.7
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(3-Aminopropyl)phenol Hydrobromide is a versatile compound widely employed in chemical synthesis for various applications. In organic chemistry, it serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. This compound can undergo various chemical reactions, such as acylation, alkylation, and oxidation, to yield a diverse range of products with unique properties. Additionally, 4-(3-Aminopropyl)phenol Hydrobromide is frequently utilized in the development of novel materials, including polymers, resins, and coatings, due to its reactivity and functional groups. Its ability to participate in multiple synthetic pathways makes it a valuable tool for researchers and chemists seeking to design and create innovative molecules with specific functionalities.