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98094-87-2

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98094-87-2 Usage

Chemical structure

1,3,8-Trihydroxy-11H-benzofuro[2,3-b][1]benzopyran-11-one

Natural occurrence

Found in plants such as soybeans, chickpeas, and fava beans

Classification

Isoflavone class of flavonoids

Health benefits

Antioxidant properties
Anti-inflammatory properties
Anticancer properties

Potential roles

Hormone regulation
Bone health

Field of interest

Natural medicine

Research focus

Therapeutic effects
Dietary supplement for various health conditions

Check Digit Verification of cas no

The CAS Registry Mumber 98094-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,0,9 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 98094-87:
(7*9)+(6*8)+(5*0)+(4*9)+(3*4)+(2*8)+(1*7)=182
182 % 10 = 2
So 98094-87-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H8O6/c16-6-1-2-8-10(4-6)20-15-12(8)14(19)13-9(18)3-7(17)5-11(13)21-15/h1-5,16-18H

98094-87-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,8-trihydroxy-[1]benzofuro[2,3-b]chromen-11-one

1.2 Other means of identification

Product number -
Other names 4',5,7-trihydroxycoumaronochromone

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:98094-87-2 SDS

98094-87-2Downstream Products

98094-87-2Relevant articles and documents

Facile synthesis of coumaronochromones through palladium-catalyzed intramolecular cross dehydrogenative coupling

Gu, Chang-Xue,Liu, Jian-Guo,Chen, Wen-Wen,Xu, Ming-Hua

, (2021/03/17)

An efficient base-free palladium-catalyzed intramolecular cross dehydrogenative coupling of 2-aryloxy substituted 4-chromenones to access coumaronochromones has been achieved. A range of diversely substituted coumaronochromones can be facilely synthesized in good to excellent yields (up to 90%).

Constrained phytoestrogens and analogues as ERβ selective ligands

Miller, Chris P.,Collini, Michael D.,Harris, Heather A.

, p. 2399 - 2403 (2007/10/03)

A new series of ERbeta (ERβ) selective ligands has been prepared. One of the compounds 6, structurally related to the phytoestrogen apigenin 4, displays a binding preference for ERβ over ERα of over 40-fold. In addition to its binding selectivity, 6 was a

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