H19808
3-Hydroxybenzaldehyde
≥99%
Synonym(s):
3-Formylphenol, 5-Hydroxybenzaldehyde, m-Formylphenol, m-Hydroxybenzaldehyde
Sign Into View Organizational & Contract Pricing
All Photos(5)
About This Item
Linear Formula:
HOC6H4CHO
CAS Number:
Molecular Weight:
122.12
Beilstein:
507099
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay:
≥99%
Recommended Products
Quality Level
Assay
≥99%
bp
191 °C/50 mmHg (lit.)
mp
100-103 °C (lit.)
SMILES string
Oc1cccc(C=O)c1
InChI
1S/C7H6O2/c8-5-6-2-1-3-7(9)4-6/h1-5,9H
InChI key
IAVREABSGIHHMO-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Application
3-Hydroxybenzaldehyde can be used as a reactant along with ethyl acetoacetate and thiourea in the synthesis of corresponding dihydropyrimidine-2-thione (monastrol), using Yb(OTf)3 as a catalyst by Biginelli cyclocondensation reaction.
It can also be used as a starting material for the synthesis of:
It can also be used as a starting material for the synthesis of:
- (-)-Quinocarcin, isoxazolo[3,4-e][2,1]benzisoxazole and 3-n-propylphenol.
- Oligo-3-hydroxybenzaldehyde (O-3HBA) by oxidative polycondensation.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Improved synthesis and preparative scale resolution of racemic monastrol
Dondoni A, et al.
Tetrahedron Letters, 43(34), 5913-5916 (2002)
A practical synthesis of 3-n-propylphenol, a component of tsetse fly attractant blends
Ujvary I and Mikite G
Organic Process Research & Development, 7(4), 585-587 (2003)
A novel cyclization to isoxazolo [3, 4-e][2, 1] benzisoxazole
Katritzky AR, et al.
Tetrahedron Letters, 43(18), 3449-3451 (2002)
Yan-Chao Wu et al.
Journal of the American Chemical Society, 130(22), 7148-7152 (2008-05-06)
(-)-Quinocarcin (1) has been synthesized in a longest linear sequence of 22 steps from 3-hydroxybenzaldehyde in 16% overall yield. The Pictet-Spengler reaction of L-tert-butyl-2-bromo-5-hydroxy phenylalanate (17), synthesized according to Corey-Lygo's enantioselective alkylation process, with benzoxyacetaldehyde (12) under mild acidic conditions
B A Stamboliyska et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 59(7), 1541-1548 (2003-04-26)
The spectral and structural changes, caused by the conversion of the 3-hydroxybenzaldehyde molecule into the corresponding oxyanion have been studied by IR spectra, and MP2 and DFT force field calculations. The conversion causes a 13 cm(-1) decrease in the frequency
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service