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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)-

Ethanol,2-[(1-methyl-2-phenoxyethyl)amino]-

OCCNC(COc1ccccc1)C Request for Quotation
Chemical Name: Ethanol,2-[(1-methyl-2-phenoxyethyl)amino]-
CAS Number: 103-39-9
Product Number: AG003G7J(AGN-PC-0OSDKD)
Synonyms:
MDL No:
Molecular Formula: C11H17NO2
Molecular Weight: 195.2582

Identification/Properties

Properties
BP:
333.5°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
195.262g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
6
Exact Mass:
195.126g/mol
Monoisotopic Mass:
195.126g/mol
Topological Polar Surface Area:
41.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
135
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#:
-
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


The molecule 2-((1-Phenoxypropan-2-yl)amino)ethanol plays a crucial role in chemical synthesis as a versatile building block. With its unique structure, it can be incorporated into various reactions to create functionalized compounds with specific properties. This compound serves as an important intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its presence enables the introduction of the phenoxy group and the aminoethyl group into target molecules, allowing for the modification of their chemical and biological activities. Additionally, 2-((1-Phenoxypropan-2-yl)amino)ethanol offers opportunities for the development of new materials and the production of advanced chemical entities. Its utility in chemical synthesis extends to diverse fields, including organic chemistry, medicinal chemistry, and materials science.