Coniferin
Title: Coniferin
CAS Registry Number: 531-29-3
CAS Name: 4-(3-Hydroxy-1-propenyl)-2-methoxyphenyl b-D-glucopyranoside
Additional Names: 4-hydroxy-3-methoxy-1-(g-hydroxypropenyl)benzene-4-D-glucoside; abietin; laricin
Molecular Formula: C16H22O8
Molecular Weight: 342.34
Percent Composition: C 56.13%, H 6.48%, O 37.39%
Literature References: Principal glucoside of the conifers. Also in comfrey root, sugar beet, and asparagus. Extraction from the cambium layer of fir: Solntsev, C.A. 38, 3780 (1944). Synthesis: Pauley, Feuerstein, Ber. 60, 1031 (1927). Hydrolysis by emulsin yields coniferyl alcohol and D-glucose. Yields lignin-like material by enzymatic dehydrogenation and polymerization: Freudenberg et al., Ber. 85, 641 (1952); Freudenberg, Rasenack, Ber. 86, 756 (1953).
 
Derivative Type: Dihydrate
Properties: Crystals from water. Anhydr after 4 hrs at 100°. Anhydr coniferin, mp 186°. [a]D20 -68° (c = 0.5). Absorption spectrum: Patterson, Hibbert, J. Am. Chem. Soc. 65, 1862 (1943). One gram dissolves in 200 ml water, freely sol in boiling water; sol in pyridine; sparingly sol in alc. Practically insol in ether.
Melting point: mp 186°
Optical Rotation: [a]D20 -68° (c = 0.5)

Others monographs:
ChlorophacinoneEtiprostonSodium PermanganatePicloram
Sodium BenzoateIbuproxamTremacamraPhenyl Tolyl Ketone
Malvidin ChlorideBoromycinDicloxacillinManganese Borate
Chloracetyl ChlorideHydrochloric AcidSodium Iodide, RadioactivePhenosulfazole
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