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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)-

2-[2-(aminomethyl)phenoxy]-N,N-dimethyl-ethanamine

NCc1ccccc1OCCN(C)C Request for Quotation
Chemical Name: 2-[2-(aminomethyl)phenoxy]-N,N-dimethyl-ethanamine
CAS Number: 91215-97-3
Product Number: AG003G8I(AGN-PC-0JOCFF)
Synonyms:
MDL No: MFCD08690290
Molecular Formula: C11H18N2O
Molecular Weight: 194.2734

Identification/Properties

Properties
BP:
89-91
Computed Properties
Molecular Weight:
194.278g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
194.142g/mol
Monoisotopic Mass:
194.142g/mol
Topological Polar Surface Area:
38.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
150
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:
Danger
UN#:
3259
Hazard Statements:
H302-H312-H314-H318-H332
Precautionary Statements:
P280-P301+P312-P301+P330+P331-P302+P352-P304+P340-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(2-(Aminomethyl)phenoxy)-N,N-dimethylethanamine, also known as $name$, is a versatile compound widely used in chemical synthesis as a key building block. This compound plays a crucial role in various organic reactions where the presence of both an amine group and a phenoxy group is required for the desired transformation. One of the primary applications of $name$ is in the synthesis of complex organic molecules such as pharmaceutical intermediates, agrochemicals, and advanced materials. Its unique structure allows for the formation of strong bonds with other functional groups, facilitating the creation of diverse chemical structures with specific properties and functions.$name$ is particularly valuable in the development of new drugs and materials that require precise control over their molecular architecture. By incorporating this compound into the synthesis process, researchers can tailor the properties of the final product to meet specific requirements, such as enhanced bioavailability, improved stability, or increased reactivity.Additionally, $name$ is instrumental in the preparation of optical isomers and chiral compounds, which are crucial in the pharmaceutical industry for producing drugs with higher efficacy and fewer side effects. Its ability to participate in asymmetric reactions makes it a valuable tool for synthesizing enantiomerically pure compounds with high selectivity.In summary, the application of 2-(2-(Aminomethyl)phenoxy)-N,N-dimethylethanamine in chemical synthesis is essential for the efficient and precise construction of complex organic molecules with tailored properties and functions. Its versatility and unique structural features make it a valuable component in the development of cutting-edge materials and pharmaceuticals with diverse applications and beneficial effects.