Glycine, N-(2-chlorobenzoyl)-


Chemical Name: Glycine, N-(2-chlorobenzoyl)-
CAS Number: 16555-60-5
Product Number: AG001W81(AGN-PC-0JNEJO)
Synonyms:
MDL No:
Molecular Formula: C9H8ClNO3
Molecular Weight: 213.6177

Identification/Properties


Properties
MP:
179-181°C
BP:
441.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
213.617g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
213.019g/mol
Monoisotopic Mass:
213.019g/mol
Topological Polar Surface Area:
66.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
232
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

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-(2-Chlorobenzamido)acetic acid plays a crucial role in chemical synthesis as a versatile building block. With its unique structure and properties, this compound is widely used for synthesizing various pharmaceuticals, agrochemicals, and materials. Its functional groups make it an essential intermediate in the production of complex organic molecules. Additionally, its reactivity allows for efficient derivatization, enabling the creation of diverse molecular structures. In the field of medicinal chemistry, 2-(2-Chlorobenzamido)acetic acid serves as a key starting material for developing new drugs and therapeutic agents. Its presence in the synthesis process enhances yields and facilitates the formation of desired products. Furthermore, its compatibility with a variety of reaction conditions makes it a valuable tool for organic chemists seeking to construct intricate molecular architectures.