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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-3-(4-methoxyphenyl)propan-1-ol

OCCC(c1ccc(cc1)OC)N Request for Quotation
Chemical Name: 3-amino-3-(4-methoxyphenyl)propan-1-ol
CAS Number: 68208-24-2
Product Number: AG005YL8(AGN-PC-0KK66N)
Synonyms:
MDL No: MFCD01863268
Molecular Formula: C10H15NO2
Molecular Weight: 181.2316

Identification/Properties

Properties
MP:
82-86°C
BP:
334.2°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
181.235g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
181.11g/mol
Monoisotopic Mass:
181.11g/mol
Topological Polar Surface Area:
55.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
133
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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-H318
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Amino-3-(4-methoxyphenyl)-1-propanol is a versatile compound widely used in chemical synthesis for various applications. Its primary role lies in serving as a key building block or intermediate in the synthesis of complex organic molecules. This compound can be utilized as a starting material or reagent in the preparation of pharmaceuticals, agrochemicals, and materials science research.In chemical synthesis, 3-Amino-3-(4-methoxyphenyl)-1-propanol can participate in a range of reactions such as reductive amination, nucleophilic substitution, and condensation reactions. Its amine functional group and aromatic moiety provide it with the necessary reactivity to undergo diverse transformations, enabling the creation of structurally intricate compounds.Specifically, 3-Amino-3-(4-methoxyphenyl)-1-propanol can be employed in the synthesis of bioactive molecules, including drug candidates and intermediates. Its presence in the molecule can impart desirable properties such as enhanced solubility, target specificity, or improved pharmacokinetic profiles. Additionally, this compound's synthetic utility extends to the preparation of specialty chemicals, dyes, and advanced materials where its unique structure can influence the properties and functions of the final product.