Detail of > 7562-61-0
- MSDS Download

- CAS Number:
- 7562-61-0
- Name:
1,3(2H,9bH)-Dibenzofurandione,2,6-diacetyl-7,9-dihydroxy-8,9b-dimethyl-, (9bR)-
- Superlist Name:
- (+)-Usniacin
- Formula:
- C18H16O7
- Molecular Structure:

- Synonyms:
- Usnic acid,(R)- (8CI);(+)-Usnic acid;(+)-Usninic acid;(R)-Usnic acid;NSC 685596;d-Usnic acid;d-Usninic acid;
- Molecular Weight:
- 344.32
- EINECS:
- 231-456-0
- Density:
- 1.49 g/cm3
- Melting Point:
- 201-203 °C(lit.)
- Boiling Point:
- 594.8 °C at 760 mmHg
- Flash Point:
- 219.1 °C
- Hazard Symbols:
Xn- Risk Codes:
- 22
- Safety:
- 36Details
- particular:
- particular
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Reference
- Extraction of (+) usnic acid
- Extraction of (+) usnic acid. (Robertet, P., et Cie., Fr.). Fr. Demande FR 2347361 4 Nov 1977, 6 pp. (French). (France). CODEN: FRXXBL. CLASS: IC: C07D307-91. APPLICATION: FR 76-11964 9 Apr 1976. DOCUMENT TYPE: Patent CA Section: 63 (Pharmaceuticals) (+)-Usnic acid (I) [7562-61-0] is extd. from the waxy residue left from lichen abs. extns. using solvents such as benzene, hexane, acetone, CHCl3, or Cl2C:CHCl. The soln. is boiled, filtered, and cooled, after which I ppts. I yields are 20-25% and 35-40% with benzene and hexane, resp. For example, waxy residue from 1 kg of oak moss from Yugoslavia or Morocco was dissolved in benzene 6L. The hot soln. was filtered and cooled using a Buchner funnel. The alc. soln. left from the abs. extn. was also filtered after being evapd. to half its original vol. A 20-25% yield of I was obtained.
- Adaptive significance of O-methylated lichen depsides and depsidones
- Adaptive significance of O-methylated lichen depsides and depsidones. Lawrey, J. D. (Dep. Bot., Ohio State Univ., Columbus, Ohio, USA). Lichenologist, 9(2), 137-42 (English) 1977. CODEN: LCHNB8. DOCUMENT TYPE: Journal CA Section: 3 (Biochemical Interactions) The O-methylated squamatic acid [569-36-8] and evernic acid [537-09-7] inhibited spore germination of Funaria hygrometrica, Ceratodon purpureus, and Mnium cuspidatum, whereas hydroxylated norstictic acid [571-67-5] and the cumarone derivs. l-usnic acid [7562-61-0] and d-usnic acid [6159-66-6] showed no inhibition of moss spore germination. O-methylated lichen depsides and depsidones are thought to be produced by morphol. advanced groups of lichens. The adaptive advantage that prodn. of O-methylated compds. confers upon lichens is possibly due to the inhibitory activity of these compds. on moss spore germination inasmuch as niche overlap between cryptogams is often considerable.
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