73151-59-4 Usage
Uses
Used in Food Industry:
(7E,9E,11E)-Aurocitrin is used as a natural food colorant for [application reason] its vibrant yellow color, providing a safe and visually appealing alternative to synthetic colorants.
Used in Pharmaceutical Industry:
(7E,9E,11E)-Aurocitrin is used as an antioxidant agent for [application reason] its ability to combat oxidative stress, which is linked to various diseases and aging.
Used in Traditional Medicine:
(7E,9E,11E)-Aurocitrin is used as a medicinal compound for [application reason] its anti-inflammatory and anti-cancer properties, which contribute to its therapeutic potential in traditional medicine.
Used in Cosmetics Industry:
(7E,9E,11E)-Aurocitrin is used as an ingredient in cosmetics for [application reason] its antioxidant and anti-inflammatory properties, which can help protect and soothe the skin.
Check Digit Verification of cas no
The CAS Registry Mumber 73151-59-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,5 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73151-59:
(7*7)+(6*3)+(5*1)+(4*5)+(3*1)+(2*5)+(1*9)=114
114 % 10 = 4
So 73151-59-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H22O3/c1-2-3-4-5-6-7-8-9-10-11-15-16(14-19)18(21)13-12-17(15)20/h6-14,20-21H,2-5H2,1H3/b7-6+,9-8+,11-10+
73151-59-4Relevant academic research and scientific papers
Access to Phenolic Fungal Metabolites via the Acid-catalysed Claisen Rearrangement. The Total Synthesis of (+/-)-Mellein, Aurocitrin, and 5',6'-Dihydroaurocitrin
Harwood, Laurence M.
, p. 2577 - 2582 (2007/10/02)
Regioselective trifluoroacetic acid catalysed rearrangement of allyl 5-allyloxy-2-hydroxybenzoate (2b) with concomitant cyclisation of the initial product permits the simple preparation of 3,4-dihydro-5,8-dihydroxy-3-methylisocoumarin (5).Hydrogenolysis of the non-hydrogen bonded hydroxy group yields (+/-)-mellein (7) whereas elaboration of the lactone moiety of compound (5) provides access to aurocitrin (8b) and its side chain analogues.
Total Synthesis of Frustulosin and Aurocitrin
Ronald, Robert C.,Lansinger, Janet M.,Lillie, Thomas S.,Wheeler, Carl J.
, p. 2541 - 2549 (2007/10/02)
The regioselective total syntheses of the novel fungal antibiotics frustulosin (1) and aurocitrin (2) were accomplished from 3,6-dihydroxy-2-iodobenzaldehyde (10) which was prepared by a regiodirected metalation of 2,5-dimethylbenzyl vinyl ether to establish the 1,2,3,4-tetrasubstitution pattern of these compounds.The unsaturated side chains of these hydroquinone antibiotics were attached by using the iodo aldehyde functionalities.The structures of these antibiotics are confirmed by synthesis.
