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Assay
98%
mp
131-134 °C (lit.)
functional group
carboxylic acid
ester
SMILES string
CC(=O)Oc1cccc(c1)C(O)=O
InChI
1S/C9H8O4/c1-6(10)13-8-4-2-3-7(5-8)9(11)12/h2-5H,1H3,(H,11,12)
InChI key
NGMYCWFGNSXLMP-UHFFFAOYSA-N
General description
3-Acetoxybenzoic acid (3-ABA), a meta-substituted benzoic acid, is an isomer of aspirin. It can be synthesized by reacting 3-hydroxybenzoic acid with acetic anhydride. The esterification of 3-ABA with 1,1′-carbonyldiimidazole (CDI) in the presence of reactive halides has been reported.
Application
3-Acetoxybenzoic acid (3-aBH) may be used as a ligand to prepare:
- bis-(3-acetoxybenzoato)triphenylantimony(V)
- bis-(3-acetoxybenzoato)triphenylbismuth(V)
- [Ln(3-ab)3(N2H4)2]·xH2O (Ln = La,Ce, Pr, Nd, Sm and Gd; N2H4= hydrazine)
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Molecules (Basel, Switzerland), 19(5), 6009-6030 (2014-05-16)
Two novel organoantimony(V) and two organobismuth(V) complexes of the type ML2 were synthesized, with L = acetylsalicylic acid (HL1) or 3-acetoxybenzoic acid (HL2) and M = triphenylantimony(V) (M1) or triphenylbismuth(V) (M2). Complexes, [M1(L1)2] (1), [M1(L2)2]∙CHCl3 (2), [M2(L1)2], (3) and [M2(L2)2]
An improved and convenient synthesis of esters using 1,1'-carbonyldiimidazole and a reactive halide.
Chemical & Pharmaceutical Bulletin, 32(12), 5044-5047 (1984)
Semi-synthesis and proteasome inhibition of D-ring deoxy analogs of (-)-epigallocatechin gallate (EGCG), the active ingredient of green tea extract.
Canadian Journal of Chemistry, 86(6), 495-502 (2008)
Hydrazine Complexes of Lanthanides with 3-Acetoxy-and 4-Acetoxybenzoic Acids: Spectroscopic, Thermal, and XRD Studies.
Journal of Chemistry, 2013 (2012)
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