Benzenecarboximidamide,4-[2-[4-(aminoiminomethyl)phenyl]ethenyl]-3-hydroxy-,dimethanesulfonate (salt)


Chemical Name: Benzenecarboximidamide,4-[2-[4-(aminoiminomethyl)phenyl]ethenyl]-3-hydroxy-,dimethanesulfonate (salt)
CAS Number: 223769-64-0
Product Number: AG00BFY4(AGN-PC-0QYZO7)
Synonyms:
MDL No: MFCD01863083
Molecular Formula: C18H24N4O7S2
Molecular Weight: 472.5358

Identification/Properties


Computed Properties
Molecular Weight:
472.531g/mol
Hydrogen Bond Donor Count:
7
Hydrogen Bond Acceptor Count:
9
Rotatable Bond Count:
4
Exact Mass:
472.109g/mol
Monoisotopic Mass:
472.109g/mol
Topological Polar Surface Area:
246A^2
Heavy Atom Count:
31
Formal Charge:
0
Complexity:
505
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
3
Compound Is Canonicalized:
Yes

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NMR Spectrum


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Chemical Structure



Hydroxystilbamidine bis(methanesulfonate) is a versatile compound commonly utilized in chemical synthesis processes. This compound serves as a key reagent for the formation of various organic molecules through the reaction with nucleophiles or electrophiles. Its unique chemical properties make it particularly valuable in the creation of complex structures and functional groups in a controlled manner. By incorporating Hydroxystilbamidine bis(methanesulfonate) into synthesis protocols, chemists can efficiently construct target molecules with high purity and yield, contributing to advancements in pharmaceuticals, materials science, and other research fields. Its application in chemical synthesis demonstrates its importance as a fundamental building block in the development of innovative compounds and materials.