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73151-59-4

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73151-59-4 Usage

General Description

"(7E,9E,11E)-Aurocitrin" is a chemical compound that belongs to the family of flavonoids. It is a natural pigment found in various plant tissues, especially in the flowers, fruits, and leaves of many plant species. Aurocitrin is known for its yellow color and is used as a natural food colorant. It also possesses antioxidant properties and has been studied for its potential health benefits, including anti-inflammatory and anti-cancer properties. Aurocitrin is also used in traditional medicine for its medicinal properties. Overall, this compound is known for its color and potential health-promoting properties.

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+

73151-59-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-dihydroxy-2-[(1E,3E,5E)-undeca-1,3,5-trienyl]benzaldehyde

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:73151-59-4 SDS

73151-59-4Downstream Products

73151-59-4Relevant articles and documents

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.

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