ethyl 2-amino-2-pyridin-2-ylacetate;dihydrochloride


Chemical Name: ethyl 2-amino-2-pyridin-2-ylacetate;dihydrochloride
CAS Number: 1236254-79-7
Product Number: AG000KW2(AGN-PC-09T3YB)
Synonyms:
MDL No: MFCD15143297
Molecular Formula: C9H14Cl2N2O2
Molecular Weight: 253.1257

Identification/Properties


Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
253.123g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
252.043g/mol
Monoisotopic Mass:
252.043g/mol
Topological Polar Surface Area:
65.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
173
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:
3
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



Ethyl 2-Amino-2-(2-pyridinyl)acetate Dihydrochloride is a versatile compound widely utilized in chemical synthesis for its diverse applications. In the field of organic chemistry, this compound serves as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity make it particularly valuable for the synthesis of complex molecules that exhibit biological activity or other desired properties.The usage of Ethyl 2-Amino-2-(2-pyridinyl)acetate Dihydrochloride in chemical synthesis is especially prominent in the pharmaceutical industry, where it is employed in the production of active pharmaceutical ingredients (APIs) for numerous therapeutic agents. This compound can undergo various reactions such as acylation, alkylation, and cyclization to afford structurally diverse compounds with potential drug-like properties. Additionally, its amino and pyridinyl functionalities offer strategic sites for further modifications, allowing for the development of novel drug candidates with enhanced pharmacological profiles.Furthermore, Ethyl 2-Amino-2-(2-pyridinyl)acetate Dihydrochloride finds applications in the synthesis of specialty chemicals, including dyes, fragrances, and agrochemicals. Its incorporation into these industries enables the creation of high-value products with specific properties tailored for a range of industrial and commercial purposes. By harnessing the synthetic capabilities of this compound, chemists can access a myriad of structural motifs that are essential for advancing chemical discovery and development efforts across various sectors.