O-iodophenols

2-Yodofenol, 98 %, Thermo Scientific Chemicals

2-Yodofenol, 98 %, Thermo Scientific Chemicals

CAS: 533-58-4 Fórmula molecular: C6H5IO Peso molecular (g/mol): 220.01 Número MDL: MFCD00013963 Clave InChI: KQDJTBPASNJQFQ-UHFFFAOYSA-N Sinónimo: 2-iodanylphenol, o-jodphenol, 2-jodfenol czech, o-jodfenol czech, phenol, iodo, 2-jodfenol, o-jodfenol, phenol, o-iodo, phenol, 2-iodo, o-iodophenol PubChem CID: 10784 ChEBI: CHEBI:16706 Nombre IUPAC: 2-yodofenol SMILES: OC1=CC=CC=C1I

4-Hidroxi-3,5-diiodobenzonitrilo, 97 %, Thermo Scientific Chemicals

4-Hidroxi-3,5-diiodobenzonitrilo, 97 %, Thermo Scientific Chemicals

CAS: 1689-83-4 Fórmula molecular: C7H3I2NO Peso molecular (g/mol): 370.92 Número MDL: MFCD00016422 Clave InChI: NRXQIUSYPAHGNM-UHFFFAOYSA-N Sinónimo: iotox, loxynil, joxynil, certrol, trevespan, cipotril, 3,5-diiodo-4-hydroxybenzonitrile, bentrol, actril, ioxynil PubChem CID: 15530 ChEBI: CHEBI:81821 Nombre IUPAC: 4-hidroxi-3,5-diiodobenzonitrilo SMILES: OC1=C(I)C=C(C=C1I)C#N

Ácido 4-hidroxi-3,5-diyodobenzoico, 97 %, Thermo Scientific Chemicals

Ácido 4-hidroxi-3,5-diyodobenzoico, 97 %, Thermo Scientific Chemicals

CAS: 618-76-8 Fórmula molecular: C7H4I2O3 Peso molecular (g/mol): 389.92 Número MDL: MFCD00016532 Clave InChI: XREKTVACBXQCSB-UHFFFAOYSA-N Sinónimo: acmc-1b674, benzoic acid, 3,5-diiodo-4-hydroxy, chembl83650, 8c0qv5jk0d, 4-hydroxy-3,5-diiodo-benzoic acid, unii-8c0qv5jk0d, benzoic acid, 4-hydroxy-3,5-diiodo, ioxynic acid, ioxynil acid, 3,5-diiodo-4-hydroxybenzoic acid PubChem CID: 12065 Nombre IUPAC: ácido 4-hidroxi-3,5-diyodobenzoico SMILES: OC(=O)C1=CC(I)=C(O)C(I)=C1

2-Yodofenol, 98 %, Thermo Scientific Chemicals

2-Yodofenol, 98 %, Thermo Scientific Chemicals

CAS: 533-58-4 Fórmula molecular: C6H5IO Peso molecular (g/mol): 220.01 Número MDL: MFCD00013963 Clave InChI: KQDJTBPASNJQFQ-UHFFFAOYSA-N Sinónimo: 2-iodanylphenol, o-jodphenol, 2-jodfenol czech, o-jodfenol czech, phenol, iodo, 2-jodfenol, o-jodfenol, phenol, o-iodo, phenol, 2-iodo, o-iodophenol PubChem CID: 10784 ChEBI: CHEBI:16706 Nombre IUPAC: 2-yodofenol SMILES: OC1=CC=CC=C1I

4-hidroxi-3-yodo-5-metoxibenzaldehído, Thermo Scientific™

4-hidroxi-3-yodo-5-metoxibenzaldehído, Thermo Scientific™

CAS: 5438-36-8 Fórmula molecular: C8H7IO3 Peso molecular (g/mol): 278.045 Clave InChI: FBBCSYADXYILEH-UHFFFAOYSA-N Sinónimo: acmc-1ao68, 5-iodo vaniline, 5-iodovanilin, 5-iodovanilline, 3-methoxy-4-hydroxy-5-iodobenzaldehyde, 5-iodo vanillin, benzaldehyde, 4-hydroxy-3-iodo-5-methoxy, 5 iodovanillin, 5-iodovanillin PubChem CID: 79499 Nombre IUPAC: 4-hidroxi-3-yodo-5-metoxibenzaldehído SMILES: COC1=C(C(=CC(=C1)C=O)I)O

5-Yodovanillina, 98 %, Thermo Scientific Chemicals

5-Yodovanillina, 98 %, Thermo Scientific Chemicals

CAS: 5438-36-8 Fórmula molecular: C8H7IO3 Peso molecular (g/mol): 278.045 Número MDL: MFCD00006941 Clave InChI: FBBCSYADXYILEH-UHFFFAOYSA-N Sinónimo: acmc-1ao68, 5-iodo vaniline, 5-iodovanilin, 5-iodovanilline, 3-methoxy-4-hydroxy-5-iodobenzaldehyde, 5-iodo vanillin, benzaldehyde, 4-hydroxy-3-iodo-5-methoxy, 5 iodovanillin, 5-iodovanillin PubChem CID: 79499 Nombre IUPAC: 4-hidroxi-3-yodo-5-metoxibenzaldehído SMILES: COC1=C(C(=CC(=C1)C=O)I)O

5-Yodovainillina, 97 %, Thermo Scientific Chemicals

5-Yodovainillina, 97 %, Thermo Scientific Chemicals

CAS: 5438-36-8 Fórmula molecular: C8H7IO3 Peso molecular (g/mol): 278.04 Número MDL: MFCD00006941 Clave InChI: FBBCSYADXYILEH-UHFFFAOYSA-N Sinónimo: acmc-1ao68, 5-iodo vaniline, 5-iodovanilin, 5-iodovanilline, 3-methoxy-4-hydroxy-5-iodobenzaldehyde, 5-iodo vanillin, benzaldehyde, 4-hydroxy-3-iodo-5-methoxy, 5 iodovanillin, 5-iodovanillin PubChem CID: 79499 Nombre IUPAC: 4-hidroxi-3-yodo-5-metoxibenzaldehído SMILES: COC1=C(C(=CC(=C1)C=O)I)O

Eritosina B, soluble en alcohol, Thermo Scientific Chemicals

Eritosina B, soluble en alcohol, Thermo Scientific Chemicals

CAS: 15905-32-5 Fórmula molecular: C20H8I4O5 Peso molecular (g/mol): 835.90 Número MDL: MFCD00005044 Clave InChI: OALHHIHQOFIMEF-UHFFFAOYSA-N Sinónimo: C.I. 45430:2; Solvent Red 140 PubChem CID: 3259 SMILES: OC1=C(I)C2=C(C=C1I)C1(OC(=O)C3=C1C=CC=C3)C1=CC(I)=C(O)C(I)=C1O2

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