tert-butyl N-ethyl-N-(2-oxoethyl)carbamate


Chemical Name: tert-butyl N-ethyl-N-(2-oxoethyl)carbamate
CAS Number: 315718-06-0
Product Number: AG00CKZP(AGN-PC-01UUEJ)
Synonyms:
MDL No:
Molecular Formula: C9H17NO3
Molecular Weight: 187.2362

Identification/Properties


Computed Properties
Molecular Weight:
187.239g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
187.121g/mol
Monoisotopic Mass:
187.121g/mol
Topological Polar Surface Area:
46.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
184
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

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Chemical Structure



Tert-Butyl ethyl(2-oxoethyl)carbamate, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in organic chemistry reactions, particularly in the formation of complex molecules. Due to its unique structure and reactivity, $name$ is commonly employed as a protecting group for sensitive functional groups during various chemical transformations.In chemical synthesis, $name$ can be utilized as a masked amine functionality, providing a strategic approach to control and manipulate specific reactions. By temporarily blocking the amine group with $name$, chemists can direct the course of a reaction towards the desired product, while ensuring the stability of the amine group under the reaction conditions. This protection-deprotection strategy enhances the selectivity and efficiency of synthetic pathways, facilitating the synthesis of intricate organic compounds.Moreover, the presence of the tert-butyl and ethyl moieties in $name$ offers additional benefits in chemical synthesis. The tert-butyl group imparts steric hindrance, influencing the regioselectivity and stereochemistry of reactions, while the ethyl group provides versatility in further functionalization. As a result, $name$ plays a crucial role in the design and synthesis of pharmaceuticals, agrochemicals, and advanced materials, enabling chemists to access a diverse array of structurally complex molecules with tailored properties.