Ethanamine, 2-(diphenylmethoxy)-N,N-dimethyl-, hydrochloride


Chemical Name: Ethanamine, 2-(diphenylmethoxy)-N,N-dimethyl-, hydrochloride
CAS Number: 147-24-0
Product Number: AG003S9A(AGN-PC-071M56)
Synonyms:
MDL No:
Molecular Formula: C17H22ClNO
Molecular Weight: 291.8157

Identification/Properties


Properties
MP:
168-172 °C
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Stability:
Light Sensitive
Refractive Index:
1.5800 (estimate)
Computed Properties
Molecular Weight:
291.819g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
6
Exact Mass:
291.139g/mol
Monoisotopic Mass:
291.139g/mol
Topological Polar Surface Area:
12.5A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
211
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


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



The compound N-(2-Diphenylmethoxyethyl)-N,N-Dimethylamine Hydrochloride, also known as $name$, serves as a versatile reagent in chemical synthesis. Its unique chemical structure enables it to participate in a variety of reactions, making it a valuable tool in organic chemistry.$name$ is commonly used as a catalyst in organic transformations due to its ability to facilitate bond formation and manipulation. Its presence can promote the formation of new carbon-carbon or carbon-heteroatom bonds, leading to the synthesis of complex organic molecules with high efficiency and selectivity.Furthermore, $name$ can also act as a protecting group in organic synthesis. By temporarily masking reactive functional groups, it enables selective reactions to occur without unwanted side reactions. This protection-deprotection strategy is crucial in the synthesis of intricate molecules where precise control over chemical reactivity is required.In addition, $name$ can serve as a chiral auxiliary in asymmetric synthesis. By incorporating this compound into a reaction, stereochemical control can be achieved, resulting in the formation of enantiomerically pure products. This is particularly important in the pharmaceutical industry, where the chirality of a molecule can significantly impact its biological activity.Overall, the application of N-(2-Diphenylmethoxyethyl)-N,N-Dimethylamine Hydrochloride in chemical synthesis spans a wide range of reactions and processes, highlighting its importance as a versatile and valuable component in the toolbox of synthetic chemists.