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3,5-Dihydroxybenzaldehyde, 98%, Thermo Scientific Chemicals
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Catalog number A15338.14
also known as A15338-14
Price (USD)/ Each
1,411.00
-
Quantity:
25 g
Price (USD)/ Each
1,411.00
3,5-Dihydroxybenzaldehyde, 98%, Thermo Scientific Chemicals
Catalog numberA15338.14
Price (USD)/ Each
1,411.00
-
Chemical Identifiers
CAS26153-38-8
IUPAC Name3,5-dihydroxybenzaldehyde
Molecular FormulaC7H6O3
InChI KeyHAQLHRYUDBKTJG-UHFFFAOYSA-N
SMILESOC1=CC(C=O)=CC(O)=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to cream
FormCrystals or powder or crystalline powder
Assay (Silylated GC)≥97.5%
3,5-Dihydroxybenzaldehyde is used as a building block in the synthesis of more complex structures. It is also used in the synthesis of terbutaline (T109750), which is an important bronchodilator.
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
3,5-Dihydroxybenzaldehyde is used as a building block in the synthesis of more complex structures. It is also used in the synthesis of terbutaline (T109750), which is an important bronchodilator.
Solubility
Soluble in ethanol and diethyl ether.
Notes
Air sensitive. Store in cool place. Incompatible with strong acids and strong bases.
3,5-Dihydroxybenzaldehyde is used as a building block in the synthesis of more complex structures. It is also used in the synthesis of terbutaline (T109750), which is an important bronchodilator.
Solubility
Soluble in ethanol and diethyl ether.
Notes
Air sensitive. Store in cool place. Incompatible with strong acids and strong bases.
RUO – Research Use Only
General References:
- Wei, J.; Li, Z.; Jin, X.; Yao, X.; Cao, X.; Chow, H.; Kuck, D. Versatile Syntheses of Hemi-Cryptophanes and a Metallo-Cryptophane from a Hexa-Functionalized C3v-Symmetrical Tribenzotriquinacene (TBTQ) Derivative. Chem. Asian J. 2015, 10 (5), 1150-1158.
- Marmisolle, W. A.; Irigoyen, J.; Gregurec, D.; Moya, S.; Azzaroni, O. Supramolecular Surface Chemistry: Substrate-Independent, Phosphate-Driven Growth of Polyamine-Based Multifunctional Thin Films. Adv. Funct. Mater. 2015, 25 (26), 4144-4152.