2-[4-(9H-fluoren-9-ylmethoxycarbonyl)morpholin-2-yl]acetic acid


Chemical Name: 2-[4-(9H-fluoren-9-ylmethoxycarbonyl)morpholin-2-yl]acetic acid
CAS Number: 885273-97-2
Product Number: AG00GRVW(AGN-PC-0GL3WW)
Synonyms:
MDL No:
Molecular Formula: C21H21NO5
Molecular Weight: 367.3951

Identification/Properties


Computed Properties
Molecular Weight:
367.401g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
367.142g/mol
Monoisotopic Mass:
367.142g/mol
Topological Polar Surface Area:
76.1A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
531
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

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



2-(4-(((9H-Fluoren-9-yl)methoxy)carbonyl)morpholin-2-yl)acetic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis processes. With its unique molecular structure, this compound plays a crucial role in various synthetic reactions, offering a range of applications in the field of chemistry.One of the key applications of $name$ in chemical synthesis is as a protecting group reagent. By selectively modifying functional groups in organic molecules, $name$ provides a protective shield during reactions, preventing unwanted side reactions or interactions. This enables chemists to manipulate specific functional groups while preserving others, facilitating the synthesis of complex molecules with precision and efficiency.Additionally, $name$ can serve as a building block in the synthesis of bioactive compounds, pharmaceuticals, and advanced materials. Its morpholin-2-yl and acetic acid functionalities make it a valuable precursor for creating diverse chemical entities with tailored properties and functions. Through strategic manipulation and derivatization, chemists can harness the reactivity of $name$ to access a wide range of structurally intricate compounds for various applications.In summary, 2-(4-(((9H-Fluoren-9-yl)methoxy)carbonyl)morpholin-2-yl)acetic acid, or $name$, is a versatile tool in chemical synthesis, offering precise functional group protection and enabling the construction of complex molecules with tailored properties. Its application in protecting group chemistry and as a building block highlights its significance in advancing synthetic methodologies and expanding the scope of chemical innovation.