83945-54-4

Basic information

• Product Name: (6R)-2-trans-2,6-dimethyl-6-hydroxy-2,7-octadienoic acid
• Synonyms: (6R)-2-trans-2,6-dimethyl-6-hydroxy-2,7-octadienoic acid
• CAS NO: 83945-54-4
• Molecular Weight: 184.235
• Mol File: 83945-54-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (6R)-2-trans-2,6-dimethyl-6-hydroxy-2,7-octadienoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (6R)-2-trans-2,6-dimethyl-6-hydroxy-2,7-octadienoic acid(83945-54-4)
• EPA Substance Registry System: (6R)-2-trans-2,6-dimethyl-6-hydroxy-2,7-octadienoic acid(83945-54-4)

Safety Data

• Hazardous Substances Data: 83945-54-4(Hazardous Substances Data)

Upstream product

• 110065-68-4 gymnocladus saponin F₁ 
• 1370004-83-3 9-(6-O-[(2E,6S)-2,6-dimethyl-6-hydroxy-2,7-octadienoyl]-β-D-glucopyranosyloxy)guaiacylglycerol 
• 1370004-84-4 9-(6-O-[(2E,6S)-2,6-dimethyl-6-hydroxy-2,7-octadienoyl]-β-D-glucopyranosyloxy)syringoylglycerol 
• 1384485-03-3 6-O-[(2E,6S)-2,6-dimethyl-6-hydroxy-2,7-octadienoyl]-(α-β)-D-glucopyranose 
• 83905-61-7 phlebotrichin 
• 92751-87-6 (6S)-2-trans-6-α-L-arabinopyranosyloxy-2,6-dimethyl-2,7-octadienoic acid 

Relevant articles and documents

A BITTER MONOTERPENE GLUCOSIDE FROM VIBURNUM PHLEBOTRICHUM

From the methanol extract of the leaves of Viburnum phlebotrichum, a new bitter monoterpene glucoside has been isolated in addition to three known compounds, p-hydroquinone, arbutin and glucoluteolin.The structures were elucidated by spectroscopic and chemical methods. - Key Word Index:Viburnum phlebotrichum; Caprifoliaceae; monoterpene glucoside; phlebotricoside.

New CuCl2-induced glucoside esters and other constituents from Portucala oleracea

Two new glucoside esters 1 and 2 were produced as stress metabolites in the fresh leaves of Portulaca oleracea, in response to abiotic stress elicitation by CuCl2. A new sugar ester (3) and two known compounds (4 and 5) were also isolated. Their structures were established by spectroscopic means. The antioxidative activities of stress metabolites and the related isolates were evaluated by DPPH assay. The results showed that new stress-driven adducts of monolignans and monoterpenes with a glucose bridge exhibited much stronger antioxidative activities than other compounds.

Studies on the constituents of leguminous plants. VI. The structure elucidations of monoterpene glycosides from fruits of Gymnocladus chinensis Baillon

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