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2,5-Dihydroxybenzaldehyde, 98+%
CAS: 1194-98-5 | C7H6O3 | 138.12 g/mol
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Catalog number A15565.03
also known as A15565-03
Price (USD)
43.65
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48.20Save 4.55 (9%)
Each
Quantity:
1 g
Price (USD)
43.65
Online Exclusive
48.20Save 4.55 (9%)
Each
Chemical Identifiers
CAS1194-98-5
IUPAC Name2,5-dihydroxybenzaldehyde
Molecular FormulaC7H6O3
InChI KeyCLFRCXCBWIQVRN-UHFFFAOYSA-N
SMILESOC1=CC=C(O)C(C=O)=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Yellow to dark green to green to brown
Melting Point (clear melt)95.0-102.0?C
FormCrystals or powder or crystalline powder
Identification (FTIR)Conforms
Assay (HPLC)≥98.0%
It is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
It is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff.
Solubility
Soluble in water.
Notes
Air sensitive. Store under inert gas. Incompatible with oxidizing agent, air.
It is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff.
Solubility
Soluble in water.
Notes
Air sensitive. Store under inert gas. Incompatible with oxidizing agent, air.
RUO – Research Use Only
General References:
- Chung-Mu Yu; Miao-Ju Yen; Lin-Chi Chen. A bioanode based on MWCNT/protein-assisted co-immobilization of glucose oxidase and 2,5-dihydroxybenzaldehyde for glucose fuel cells. Biosensors and Bioelectronics. 2010, 25 (11), 2515-2521.
- Javed Iqbal; Neelima D Tangellamudi; Balakrishna Dulla; Sridhar Balasubramanian. Sequential C-N and C-O bond formation in a single pot: synthesis of 2H-benzo[b][1,4]oxazines from 2,5-dihydroxybenzaldehyde and amino acid precursors. Organic Letters. 2012, 14, (2), 552-555.
- Has been converted conveniently in 4 steps to 4,7-dibenzyloxyindole via the Nenitzescu indole synthesis (Henry reaction with Nitromethane, A11806). The product is a precursor of pyrroloquinoline alkaloids: Synlett, 755 (1993).