4-(Aminomethyl)benzoic Acid
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4-(Aminomethyl)benzoic Acid

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4-(Aminomethyl)benzoic Acid, an unnatural amino acid derivative, is a type 2 antifibrinolytic agent,

Category
Cyclic Amino Acids
Catalog number
BAT-008123
CAS number
56-91-7
Molecular Formula
C8H9NO2
Molecular Weight
151.16
4-(Aminomethyl)benzoic Acid
IUPAC Name
4-(aminomethyl)benzoic acid
Synonyms
4-(Aminomethyl)benzoic Acid; Tranexamic Acid Impurity D, α-Amino-p-toluic Acid
Appearance
White Solid
Purity
≥95%
Density
1.239g/cm3
Melting Point
276-280 °C
Boiling Point
323.1°C at 760mmHg
Storage
Store at -20 °C
Solubility
Soluble in DMSO
InChI
1S/C8H9NO2/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4H,5,9H2,(H,10,11)
InChI Key
QCTBMLYLENLHLA-UHFFFAOYSA-N
Canonical SMILES
C1=CC(=CC=C1CN)C(=O)O
1.Synthesis of polymer-bound 4-acetoxy-3-phenylbenzaldehyde derivatives: applications in solid-phase organic synthesis.
Kumar A1, Ye G, Ahmadibeni Y, Parang K. J Org Chem. 2006 Sep 29;71(20):7915-8.
Aminomethyl polystyrene resin was reacted with 4-(5'-formyl-2'-hydroxyphenyl)benzoic acid and 4-(5'-formyl-2'-hydroxyphenyl)phenyl propionic acid, respectively, in the presence of 1-hydroxybenzotriazole and 1,3-diisopropylcarbodiimide to yield polymer-bound benzaldehydes. The phenolic group in resins was acetylated with acetic anhydride to afford two polymer-bound 4-acetoxybenzaldehydes. The reductive amination of polymer-bound linkers by amines and sodium triacetoxyborohydride, followed by sulfonylation with arylsulfonyl chloride derivatives in the presence of pyridine and the cleavage with TFA/DCM/H2O, produced pure sulfonamides.
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