CAS RN 118-41-2
Ácido 3,4,5-tricloroacético, +99 %, Thermo Scientific Chemicals
CAS: 118-41-2 Fórmula molecular: C10H12O5 Peso molecular (g/mol): 212.2 Número MDL: MFCD00002501 Clave InChI: SJSOFNCYXJUNBT-UHFFFAOYSA-N Sinónimo: eudesmic acid,gallic acid trimethyl ether,tri-o-methylgallic acid,trimethylgallic acid,benzoic acid, 3,4,5-trimethoxy,veratric acid, 5-methoxy,unii-v5c9h0sc9f,3,4,5-trimethoxy-benzoic acid,5-methoxy-veratric acid,v5c9h0sc9f PubChem CID: 8357 ChEBI: CHEBI:454991 Nombre IUPAC: ácido 3,4,5-trimetoxibenzoico SMILES: COC1=CC(=CC(OC)=C1OC)C(O)=O
Ácido 3,4,5-trimetoxibenzoico, +99 %, Thermo Scientific Chemicals
CAS: 118-41-2 Fórmula molecular: C10H12O5 Peso molecular (g/mol): 212.2 Número MDL: MFCD00002501 Clave InChI: SJSOFNCYXJUNBT-UHFFFAOYSA-N Sinónimo: eudesmic acid,gallic acid trimethyl ether,tri-o-methylgallic acid,trimethylgallic acid,benzoic acid, 3,4,5-trimethoxy,veratric acid, 5-methoxy,unii-v5c9h0sc9f,3,4,5-trimethoxy-benzoic acid,5-methoxy-veratric acid,v5c9h0sc9f PubChem CID: 8357 ChEBI: CHEBI:454991 Nombre IUPAC: ácido 3,4,5-trimetoxibenzoico SMILES: COC1=CC(=CC(OC)=C1OC)C(O)=O
Ácido 3,4,5-Trimetoxibenzoico, TRC
CAS: 118-41-2 Fórmula molecular: C10 H12 O5 Peso molecular (g/mol): 212.2 Sinónimo: 3,4,5-Trimethoxybenzoic Acid,Trimebutine Imp. B (EP),Trimethoprim Imp. J (EP),Benzoic acid, 3,4,5-trimethoxy- (7CI, 8CI, 9CI, ACI),3,4,5-Trimethoxybenzoic acid (ACI),Eudesmic acid,Gallic acid trimethyl ether,NSC 2525,Tri-O-methylgallic acid,Trimethylgallic acid Nombre IUPAC: ácido 3,4,5-trimetoxibenzoico SMILES: COc1cc(cc(OC)c1OC)C(=O)O
Ácido 3,4,5-trimetoxibenzoico, Mikromol™
Descubrir Mikromol - su fuente confiable de estándares de referencia farmacéuticos de alta calidad. Apoyando un análisis preciso y conforme con las normas ISO Materiales acreditados 17034 diseñados para brindar confianza en cada resultado.
3,4,5-Trimethoxybenzoic acid, MedChemExpress
MedChemExpress 3,4,5-Trimethoxybenzoic acid (Eudesmic acid;Trimethylgallic Acid) is a benzoic acid derivative. A building block in medicine and organic synthesis.