2-Hydroxy-5-methoxybenzaldehyde

2-Hydroxy-5-methoxybenzaldehyde
Names
	Preferred IUPAC name 2-Hydroxy-5-methoxybenzaldehyde
	Other names 5-Methoxysalicylaldehyde; 2-Formyl-4-methoxyphenol; 6-Hydroxy-m-anisaldehyde
Identifiers
CAS Number	672-13-9 ;
3D model (JSmol)	Interactive image;
ChemSpider	21168855 ;
ECHA InfoCard	100.010.537
EC Number	211-589-0;
PubChem CID	24848799;
UNII	GYT2Q9UR3W ;
CompTox Dashboard (EPA)	DTXSID40217478 ;
	InChI InChI=1S/C9H10O3/c1-11-8-3-4-9(12-2)7(5-8)6-10/h3-6H,1-2H3 Key: FZHSPPYCNDYIKD-UHFFFAOYSA-N ; InChI=1S/C8H8O3/c1-11-7-2-3-8(10)6(4-7)5-9/h2-5,10H,1H3 Key: AFUKNJHPZAVHGQ-UHFFFAOYAN;
	SMILES COC1=CC(=C(C=C1)O)C=O;
Properties
Chemical formula	C8H8O3
Molar mass	152.149 g·mol−1
Appearance	Yellow to yellow-green liquid
Density	1.219 g/mL
Melting point	4 °C (39 °F; 277 K)
Boiling point	250 °C (482 °F; 523 K)
Refractive index (nD)	1.578
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

2-Hydroxy-5-methoxybenzaldehyde is an organic compound and an isomer of vanillin.

Synthesis and reactions

The chemical is produced by the Reimer-Tiemann reaction on 4-methoxyphenol with a 79% yield.^[1]

It reacts with malononitrile to form 2-imino-6-methoxy-2H-1-benzopyran-3-carbonitrile.^[2] It can be reduced by sodium borohydride in ethanol to form 2-hydroxy-5-methoxybenzyl alcohol.^[3]

References

^ Wynberg, Hans; Meijer, Egbert W. (2005). The Reimer–Tiemann Reaction. p. 16. doi:10.1002/0471264180.or028.01. ISBN 9780471264187.
^ Dinparast, Leila; Hemmati, Salar; Zengin, Gokhan; Alizadeh, Ali Akbar; Bahadori, Mir Babak; Kafil, Hossein Samadi; Dastmalchi, Siavoush (2019). "Rapid, Efficient, and Green Synthesis of Coumarin Derivatives via Knoevenagel Condensation and Investigating Their Biological Effects". ChemistrySelect. 4 (31): 9211–9215. doi:10.1002/slct.201901921. ISSN 2365-6549. S2CID 202077668.
^ Cheng, Yan; Ono, Masahiro; Kimura, Hiroyuki; Kagawa, Shinya; Nishii, Ryuichi; Kawashima, Hidekazu; Saji, Hideo (2010). "Fluorinated Benzofuran Derivatives for PET Imaging of β-Amyloid Plaques in Alzheimer's Disease Brains". ACS Medicinal Chemistry Letters. 1 (7): 321–325. doi:10.1021/ml100082x. ISSN 1948-5875. PMC 4007906. PMID 24900214.

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[1] Wynberg, Hans; Meijer, Egbert W. (2005). The Reimer–Tiemann Reaction. p. 16. doi:10.1002/0471264180.or028.01. ISBN 9780471264187.

[2] Dinparast, Leila; Hemmati, Salar; Zengin, Gokhan; Alizadeh, Ali Akbar; Bahadori, Mir Babak; Kafil, Hossein Samadi; Dastmalchi, Siavoush (2019). "Rapid, Efficient, and Green Synthesis of Coumarin Derivatives via Knoevenagel Condensation and Investigating Their Biological Effects". ChemistrySelect. 4 (31): 9211–9215. doi:10.1002/slct.201901921. ISSN 2365-6549. S2CID 202077668.

[3] Cheng, Yan; Ono, Masahiro; Kimura, Hiroyuki; Kagawa, Shinya; Nishii, Ryuichi; Kawashima, Hidekazu; Saji, Hideo (2010). "Fluorinated Benzofuran Derivatives for PET Imaging of β-Amyloid Plaques in Alzheimer's Disease Brains". ACS Medicinal Chemistry Letters. 1 (7): 321–325. doi:10.1021/ml100082x. ISSN 1948-5875. PMC 4007906. PMID 24900214.

[1]

[2]

[3]

Synthesis and reactions

See also

References