1,2-Azetidinedicarboxylic acid, 1-(1,1-dimethylethyl) 2-methyl ester


Chemical Name: 1,2-Azetidinedicarboxylic acid, 1-(1,1-dimethylethyl) 2-methyl ester
CAS Number: 255882-72-5
Product Number: AG003S1A(AGN-PC-002O08)
Synonyms:
MDL No: MFCD06657099
Molecular Formula: C10H17NO4
Molecular Weight: 215.2463

Identification/Properties


Properties
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
215.249g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
215.116g/mol
Monoisotopic Mass:
215.116g/mol
Topological Polar Surface Area:
55.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
269
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

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NMR Spectrum


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Chemical Structure



1,​2-​Azetidinedicarboxyli​c acid, 1-​(1,​1-​dimethylethyl) 2-​methyl ester, commonly known as $name$, plays a crucial role in modern chemical synthesis processes. With its unique chemical properties, this compound is utilized as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. In chemical synthesis, $name$ serves as a versatile intermediate that can undergo various functional group transformations, allowing for the efficient incorporation of its structural elements into more complex molecules. Its bicyclic ring structure provides a solid framework for further modifications, enabling the synthesis of novel compounds with desired properties.$name$ is particularly valued for its ability to introduce specific functionalities, such as carboxylic acid and ester groups, into target molecules with precision. This capability makes it a valuable tool in the development of potent pharmaceutical agents and biologically active compounds. Additionally, the presence of the tert-butyl and methyl substituents in $name$ confers stability and sterically hinders certain reactions, thereby directing selectivity in synthesis pathways.Overall, the application of 1,​2-​Azetidinedicarboxyli​c acid, 1-​(1,​1-​dimethylethyl) 2-​methyl ester in chemical synthesis showcases its importance as a versatile and reliable building block for creating diverse and valuable chemical compounds.