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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzoic acid, 2-[(2-furanylmethyl)amino]-

OC(=O)c1ccccc1NCc1ccco1 Request for Quotation
Chemical Name: Benzoic acid, 2-[(2-furanylmethyl)amino]-
CAS Number: 501661-50-3
Product Number: AG00I8YQ(AGN-PC-0JM8T8)
Synonyms:
MDL No:
Molecular Formula: C12H11NO3
Molecular Weight: 217.2206

Identification/Properties

Computed Properties
Molecular Weight:
217.224g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
217.074g/mol
Monoisotopic Mass:
217.074g/mol
Topological Polar Surface Area:
62.5A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
244
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


2-((Furan-2-ylmethyl)amino)benzoic acid, or $name$, serves as a versatile building block in chemical synthesis due to its unique molecular structure. This compound is commonly employed as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. By utilizing $name$ as a starting material, chemists can efficiently access a wide array of complex molecules through strategic functional group manipulations. Its strategic placement of functional groups makes it a valuable tool for introducing both furan and amino moieties into target molecules, enabling the synthesis of diverse compounds with tailored properties and functionalities. Additionally, the presence of the benzoic acid group in $name$ offers further synthetic flexibility, allowing for the incorporation of this moiety into the final products for enhanced chemical reactivity or biological activity. Overall, the application of 2-((Furan-2-ylmethyl)amino)benzoic acid in chemical synthesis enables researchers to access novel compounds with potential applications in various industries.