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

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 
• 92751-87-6 (6S)-2-trans-6-α-L-arabinopyranosyloxy-2,6-dimethyl-2,7-octadienoic acid 
• 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 

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.

α-Glucosidic hydroquinone derivatives from Viburnum erosum

Six undescribed compounds (1–6) were isolated from the leaves of Viburnum erosum along with four known compounds 7–10. The structures were determined by NMR and MS spectroscopic analyses, and their absolute configurations were established by chemical and

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. X. The Structures of New Triterpenoid Saponins from the Fruits of Gymnocladus chinensis BAILLON

Four new triterpenoid saponins, gymnocladus saponins F2 (1), F1 (2), E (3) and D1 (4), were isolated from the fruits of Gymnocladus chinensis BAILLON.On the basis of chemical and physicochemical evidence, they were characterized structurally as 3,28-bisglycosides of 2β,23-dihydroxyacacic acid having a glycosyl monoterpene carboxylate as an acyl moiety.