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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)-

(3S)-3-amino-3-(3-methoxyphenyl)propan-1-ol

OCCC(c1cccc(c1)OC)N Request for Quotation
Chemical Name: (3S)-3-amino-3-(3-methoxyphenyl)propan-1-ol
CAS Number: 22490-86-4
Product Number: AG00C1C6(AGN-PC-05CJF4)
Synonyms:
MDL No:
Molecular Formula: C10H15NO2
Molecular Weight: 181.2316

Identification/Properties

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:
141
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:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Amino-3-(3-methoxyphenyl)propan-1-ol is a versatile compound that finds valuable application in chemical synthesis processes. Known for its unique structure and reactivity, this compound serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and materials.One significant application of 3-Amino-3-(3-methoxyphenyl)propan-1-ol is its role as a building block in the synthesis of biologically active compounds. By utilizing its amine and alcohol functional groups, chemists can modify the structure of this compound to introduce specific functionalities that are crucial for designing new drugs or agrochemicals. This compound acts as a scaffold upon which various chemical transformations can be performed to create new molecules with desired properties.Furthermore, 3-Amino-3-(3-methoxyphenyl)propan-1-ol can participate in reactions like reductive amination, acylation, and nucleophilic substitution, enabling chemists to access structurally diverse compounds efficiently. Its ability to undergo multiple types of reactions makes it a valuable tool in the synthesis of complex organic molecules.Overall, 3-Amino-3-(3-methoxyphenyl)propan-1-ol plays a crucial role in chemical synthesis by serving as a versatile building block for the construction of diverse compounds with applications across various industries. Its reactivity and unique structure make it an indispensable component in the toolkit of synthetic chemists.