Hydrazinecarboxylic acid, (4-methoxyphenyl)methyl ester


Chemical Name: Hydrazinecarboxylic acid, (4-methoxyphenyl)methyl ester
CAS Number: 18912-37-3
Product Number: AG002HX4(AGN-PC-0JLX2E)
Synonyms:
MDL No:
Molecular Formula: C9H12N2O3
Molecular Weight: 196.2032

Identification/Properties


Properties
Storage:
Light sensitive;Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
196.206g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
196.085g/mol
Monoisotopic Mass:
196.085g/mol
Topological Polar Surface Area:
73.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
179
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



4-Methoxybenzyl hydrazinecarboxylate, also known as MBHC, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the development of various pharmaceuticals, agrochemicals, and materials due to its unique reactivity and structural properties. In chemical synthesis, 4-Methoxybenzyl hydrazinecarboxylate is commonly employed as a valuable intermediate in the production of heterocyclic compounds and complex organic molecules. It participates in a range of reactions including acylation, alkylation, condensation, and cyclization processes. Due to its hydrazine functionality, MBHC offers a reactive site for the formation of C-N bonds, enabling the incorporation of nitrogen atoms into molecular frameworks. This property makes it particularly useful in the synthesis of nitrogen-containing compounds such as pyrazoles, pyridazines, and hydrazones.Moreover, the methoxybenzyl group in this compound provides stability and protection to sensitive functional groups during synthetic transformations. This feature allows for selective modifications and controlled manipulations in multi-step synthesis routes, facilitating the construction of complex chemical structures.Overall, 4-Methoxybenzyl hydrazinecarboxylate plays a pivotal role in the realm of chemical synthesis, enabling the efficient and strategic construction of diverse organic molecules with significant applications in drug discovery, materials science, and agrochemical development.