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7,4'-Dihydroxyflavan, also known as Leucodelphinidin, is a type of flavan, a subgroup of flavonoids, which are naturally occurring compounds found in plants. These compounds are known for their antioxidant properties and are often associated with the health benefits of consuming fruits, vegetables, and other plant-based foods. 7,4'-Dihydroxyflavan specifically has a unique structure with hydroxyl groups at the 7 and 4' positions, which may contribute to its potential biological activities. It is part of a larger class of compounds that are being studied for their potential roles in health and disease prevention, including their effects on inflammation, cardiovascular health, and cancer prevention. The study of flavans like 7,4'-Dihydroxyflavan is an active area of research in the field of natural products chemistry and pharmacology.

494-48-4

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494-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 494-48-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 494-48:
(5*4)+(4*9)+(3*4)+(2*4)+(1*8)=84
84 % 10 = 4
So 494-48-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O3/c16-12-5-1-10(2-6-12)14-8-4-11-3-7-13(17)9-15(11)18-14/h1-3,5-7,9,14,16-17H,4,8H2

494-48-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-7-ol

1.2 Other means of identification

Product number -
Other names 7,4'-Dihydroxyflavan

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:494-48-4 SDS

494-48-4Downstream Products

494-48-4Relevant academic research and scientific papers

USE OF HYDROXYFLAVAN DERIVATIVES FOR TASTE MODIFICATION

-

, (2010/12/18)

The present invention primarily relates to the use of specific compounds of formula (I) or of specific salts of a compound of formula (I) or mixtures thereof for synergistically enhancing the sweet taste of a sweet-tasting substance.

Simplified YM-26734 inhibitors of secreted phospholipase A2 group IIA

Oslund, Rob C.,Cermak, Nathan,Verlinde, Christophe L.M.J.,Gelb, Michael H.

supporting information; experimental part, p. 5415 - 5419 (2009/05/30)

Simplified analogs of YM-26734, a known inhibitor of secreted phospholipase A2 (sPLA2) group IIA, were synthesized and found to also display potent inhibition at low nanomolar concentrations. Analogs were based on the didodecanoylphl

Studies on flavans. III. The total synthesis of (±)-7,4′ -dihydroxy-3′-methoxyflavan, (±)-7,3′-dihydroxy-4′ -methoxyflavan, and (±)-7,4′-dihdroxyflavan

Xue, Jijun,Zhang, Xianshu,Chen, Xuesong,Zhang, Yingpeng,Li, Ying

, p. 3527 - 3536 (2007/10/03)

The first total synthesis of (±)-7,3′-dihydroxy-4′ -methoxyflavan (1) and (±)-7,4′-dihydroxy-3′-methoxyflavan (2), along with the synthesis of (±)-7,4′-dihydroxyflavan (3), three naturally occurring flavans, were described. The key step is the cyclization of 1,3-diaryl-1-propanol by BF3·Et2O.

Identification of three hydroxyflavan phytoalexins from daffodil bulbs

Coxon, David T.,O'Neill, Timothy M.,Mansfield, John W.,Porter, Alexander E.A.

, p. 889 - 891 (2007/10/02)

Three phytoalexins were isolated from daffodil bulb scales inoculated with Botrytis cinerea and identified as 7-hydroxyflavan, 7,4′-dihydroxyflavan and 7,4′-dihydroxy-8-methylflavan. The structures of the phytoalexins were confirmed by total synthesis.

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