Coniferyl alcohol

Coniferyl alcohol
Names
	Preferred IUPAC name 4-[(1E)-3-Hydroxyprop-1-en-1-yl]-2-methoxyphenol
	Other names 4-hydroxy-3-methoxycinnamyl alcohol; Coniferol
Identifiers
CAS Number	458-35-5 ;
3D model (JSmol)	Interactive image;
Beilstein Reference	2048963
ChEBI	CHEBI:17745 ;
ChEMBL	ChEMBL501870 ;
ChemSpider	1266063 ;
ECHA InfoCard	100.260.977
EC Number	207-277-9;
KEGG	C00590;
PubChem CID	1549095;
UNII	E7SM92591P ;
CompTox Dashboard (EPA)	DTXSID50186489 ;
	InChI InChI=1S/C10H12O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h2-5,7,11-12H,6H2,1H3/b3-2+ Key: JMFRWRFFLBVWSI-NSCUHMNNSA-N ; InChI=1/C10H12O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h2-5,7,11-12H,6H2,1H3/b3-2+ Key: JMFRWRFFLBVWSI-NSCUHMNNBF;
	SMILES Oc1ccc(cc1OC)/C=C/CO;
Properties
Chemical formula	C10H12O3
Molar mass	180.203 g·mol−1
Melting point	74 °C (165 °F; 347 K)
Boiling point	163 to 165 °C (325 to 329 °F; 436 to 438 K)
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H315, H319, H335
Precautionary statements	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
	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

Coniferyl alcohol is an organic compound with the formula HO(CH₃O)C₆H₃CH=CHCH₂OH. A colourless or white solid, it is one of the monolignols, produced via the phenylpropanoid biochemical pathway. When copolymerized with related aromatic compounds, coniferyl alcohol forms lignin or lignans.^[1]^[2]^[3] Coniferin is a glucoside of coniferyl alcohol. Coniferyl alcohol is an intermediate in biosynthesis of eugenol and of stilbenoids and coumarin. Gum benzoin contains significant amount of coniferyl alcohol and its esters. It is found in both gymnosperm and angiosperm plants. Sinapyl alcohol and paracoumaryl alcohol, the other two lignin monomers, are found in angiosperm plants and grasses.

Occurrence

Coniferyl alcohol is produced from coniferyl aldehyde by the action of dehydrogenase enzymes.^[3]

It is a queen retinue pheromone (QRP), a type of honey bee pheromone found in the mandibular glands.^[4]

In Forsythia intermedia a dirigent protein was found to direct the stereoselective biosynthesis of (+)-pinoresinol from coniferyl alcohol.^[5] Recently, a second, enantiocomplementary dirigent protein was identified in Arabidopsis thaliana, which directs enantioselective synthesis of (−)-pinoresinol.^[6]

References

^ Iiyama, Kenji; Lam, Thi Bach-Tuyet; Stone, Bruce A. (1994). "Covalent Cross-Links in the Cell Wall". Plant Physiology. 104 (2): 315–320. doi:10.1104/pp.104.2.315. PMC 159201. PMID 12232082.
^ Wout Boerjan, John Ralph, Marie Baucher "Lignin Biosynthesis" Annu. Rev. Plant Biol. 2003, vol. 54, pp. 519–46. doi:10.1146/annurev.arplant.54.031902.134938
^ ^a ^b Li, Laigeng; Cheng, Xiao Fei; Leshkevich, Jacqueline; Umezawa, Toshiaki; Harding, Scott A.; Chiang, Vincent L. (2001). "The Last Step of Syringyl Monolignol Biosynthesis in Angiosperms is Regulated by a Novel Gene Encoding Sinapyl Alcohol Dehydrogenase". The Plant Cell. 13 (7): 1567–1586. doi:10.1105/tpc.010111. PMC 139549. PMID 11449052.
^ Keeling, C. I.; Slessor, K. N.; Higo, H. A.; Winston, M. L. (2003). "Isolation and identification of new components of the honey bee (Apis mellifera L.) queen retinue pheromone". Proc. Natl. Acad. Sci. U.S.A. 100 (8): 4486–4491. Bibcode:2003PNAS..100.4486K. doi:10.1073/pnas.0836984100. PMC 153582. PMID 12676987.
^ Davin, L. B.; Wang, H. B.; Crowell, A. L.; et al. (1997). "Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center". Science. 275 (5298): 362–366. doi:10.1126/science.275.5298.362. PMID 8994027. S2CID 41957412.
^ Pickel, B.; Constantin, M.-A.; Pfannsteil, J.; Conrad, J.; Beifuss, U.; Schaffer, A. (March 2007). "An Enantiocomplementary Dirigent Protein for the Enantioselective Laccase-Catalyzed Oxidative Coupling of Phenols". Angewandte Chemie. 53 (4): 273–284. doi:10.1007/s10086-007-0892-x. S2CID 195313754.

[1] Iiyama, Kenji; Lam, Thi Bach-Tuyet; Stone, Bruce A. (1994). "Covalent Cross-Links in the Cell Wall". Plant Physiology. 104 (2): 315–320. doi:10.1104/pp.104.2.315. PMC 159201. PMID 12232082.

[2] Wout Boerjan, John Ralph, Marie Baucher "Lignin Biosynthesis" Annu. Rev. Plant Biol. 2003, vol. 54, pp. 519–46. doi:10.1146/annurev.arplant.54.031902.134938

[PNAS-3] Li, Laigeng; Cheng, Xiao Fei; Leshkevich, Jacqueline; Umezawa, Toshiaki; Harding, Scott A.; Chiang, Vincent L. (2001). "The Last Step of Syringyl Monolignol Biosynthesis in Angiosperms is Regulated by a Novel Gene Encoding Sinapyl Alcohol Dehydrogenase". The Plant Cell. 13 (7): 1567–1586. doi:10.1105/tpc.010111. PMC 139549. PMID 11449052.

[4] Keeling, C. I.; Slessor, K. N.; Higo, H. A.; Winston, M. L. (2003). "Isolation and identification of new components of the honey bee (Apis mellifera L.) queen retinue pheromone". Proc. Natl. Acad. Sci. U.S.A. 100 (8): 4486–4491. Bibcode:2003PNAS..100.4486K. doi:10.1073/pnas.0836984100. PMC 153582. PMID 12676987.

[5] Davin, L. B.; Wang, H. B.; Crowell, A. L.; et al. (1997). "Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center". Science. 275 (5298): 362–366. doi:10.1126/science.275.5298.362. PMID 8994027. S2CID 41957412.

[6] Pickel, B.; Constantin, M.-A.; Pfannsteil, J.; Conrad, J.; Beifuss, U.; Schaffer, A. (March 2007). "An Enantiocomplementary Dirigent Protein for the Enantioselective Laccase-Catalyzed Oxidative Coupling of Phenols". Angewandte Chemie. 53 (4): 273–284. doi:10.1007/s10086-007-0892-x. S2CID 195313754.

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v t e Types of monolignols
Aglycones	coniferyl alcohol sinapyl alcohol paracoumaryl alcohol
Glycosides	Coniferin

v t e Types of phenylpropanoids
Classes of phenylpropanoids	Hydroxycinnamic acids Chromones (Furanochromones) Cinnamaldehydes Monolignols Coumarins Chalcones Flavonoids Allylbenzenes Stilbenoids Lignans Lignins Suberins
Examples	Rhododendrin