H19808
3-Hydroxybenzaldehyde
≥99%
Synonym(s):
3-Formylphenol, 5-Hydroxybenzaldehyde, m-Formylphenol, m-Hydroxybenzaldehyde
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
HOC6H4CHO
CAS Number:
Molecular Weight:
122.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-892-9
Beilstein/REAXYS Number:
507099
MDL number:
Assay:
≥99%
InChI key
IAVREABSGIHHMO-UHFFFAOYSA-N
InChI
1S/C7H6O2/c8-5-6-2-1-3-7(9)4-6/h1-5,9H
SMILES string
Oc1cccc(C=O)c1
assay
≥99%
bp
191 °C/50 mmHg (lit.)
Quality Level
Looking for similar products? Visit Product Comparison Guide
Related Categories
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
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.
A novel cyclization to isoxazolo [3, 4-e][2, 1] benzisoxazole
Katritzky AR, et al.
Tetrahedron Letters, 43(18), 3449-3451 (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)
Improved synthesis and preparative scale resolution of racemic monastrol
Dondoni A, et al.
Tetrahedron Letters, 43(34), 5913-5916 (2002)
The synthesis and thermal properties of oligo-3-hydroxybenzaldehyde synthesized by oxidative polycondensation
Mart H, et al.
Journal of Applied Polymer Science, 101(2), 892-897 (2006)
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
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