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3-Hydroxy-9,10-(2,2-dimethyl-1-oxabutane-1,4-diyl)-6H-benzofuro[3,2-c][1]benzopyran-6-one, also known as a coumestan, is a naturally occurring compound belonging to the class of coumestans. It is characterized by the presence of a hydroxy group at position 3 and a 2,2-dimethylpyran group across positions 9 and 10. This unique structure endows it with potential biological activities and applications in various fields.

18979-00-5

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18979-00-5 Usage

Uses

Used in Pharmaceutical Industry:
3-Hydroxy-9,10-(2,2-dimethyl-1-oxabutane-1,4-diyl)-6H-benzofuro[3,2-c][1]benzopyran-6-one is used as a pharmaceutical agent for its potential therapeutic properties. Its unique structure allows it to interact with various biological targets, making it a promising candidate for the development of new drugs.
Used in Nutraceutical Industry:
In the nutraceutical industry, 3-Hydroxy-9,10-(2,2-dimethyl-1-oxabutane-1,4-diyl)-6H-benzofuro[3,2-c][1]benzopyran-6-one is used as a dietary supplement due to its potential health benefits. Its presence in certain plant sources suggests that it may contribute to the overall health-promoting effects of these plants.
Used in Cosmetic Industry:
3-Hydroxy-9,10-(2,2-dimethyl-1-oxabutane-1,4-diyl)-6H-benzofuro[3,2-c][1]benzopyran-6-one is used as an active ingredient in cosmetic products for its potential skin health benefits. Its unique structure may provide antioxidant and anti-inflammatory properties, which can contribute to improved skin health and appearance.
Used in Agricultural Industry:
In the agricultural industry, 3-Hydroxy-9,10-(2,2-dimethyl-1-oxabutane-1,4-diyl)-6H-benzofuro[3,2-c][1]benzopyran-6-one is used as a natural pesticide or growth promoter. Its potential biological activities may help protect crops from pests and diseases, as well as promote healthy growth and yield.
Overall, the diverse applications of 3-Hydroxy-9,10-(2,2-dimethyl-1-oxabutane-1,4-diyl)-6H-benzofuro[3,2-c][1]benzopyran-6-one highlight its potential as a versatile compound with significant benefits across various industries. Further research and development are needed to fully explore and harness its potential for the betterment of human health, agriculture, and other fields.

Check Digit Verification of cas no

The CAS Registry Mumber 18979-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,7 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18979-00:
(7*1)+(6*8)+(5*9)+(4*7)+(3*9)+(2*0)+(1*0)=155
155 % 10 = 5
So 18979-00-5 is a valid CAS Registry Number.

18979-00-5SDS

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 sojagol

1.2 Other means of identification

Product number -
Other names Soyagol

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:18979-00-5 SDS

18979-00-5Downstream Products

18979-00-5Relevant academic research and scientific papers

ISOSOJAGOL, A COUMESTAN FROM PHASEOLUS COCCINEUS

O'Neill, Melanie J.,Adesanya, S. A.,Roberts, Margaret F.

, p. 2704 - 2705 (1984)

A novel coumestan isolated from Phaseolus coccineus has been characterized as 3,9-dihydroxy-10-(γ,γ-dimethylallyl)-coumestan and named isosojagol.Key Word Index - Phaseolus coccineus; Leguminosae; coumestan; isosojagol.

Total synthesis of the antibiotic erypoegin H and cognates by a PtCl 2-catalyzed cycloisomerization reaction

Fuerstner, Alois,Heilmann, Eike K.,Davies, Paul W.

, p. 4760 - 4763 (2008/02/08)

(Chemical Equation Presented) Fighting back: A concise route to the pterocarpene derivative erypoegin H, a natural product endowed with considerable activity against a range of methicillin-resistant Staphyllococcus aureus strains and vancomycin-resistant

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