Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2',7-Dihydroxy-4'-methoxyisoflavan, a natural chemical compound within the isoflavonoid group, is characterized by the presence of two hydroxyl groups at the 2' and 7 positions and a methoxy group at the 4' position on its structure. It is commonly found in a variety of plants and vegetables and is known for its antioxidant and anti-inflammatory properties. 2',7-DIHYDROXY-4'-METHOXYISOFLAVAN has garnered interest for its potential health benefits, including disease prevention and treatment, as well as its possible role in cancer prevention, treatment, and hormone-related conditions due to its structural resemblance to estrogen. As a result, 2',7-dihydroxy-4'-methoxyisoflavan is a promising candidate for further research in the fields of natural products and medicinal chemistry.

56701-24-7

Post Buying Request

56701-24-7 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

56701-24-7 Usage

Uses

Used in Pharmaceutical Applications:
2',7-Dihydroxy-4'-methoxyisoflavan is used as a potential therapeutic agent for various diseases due to its antioxidant and anti-inflammatory properties. Its ability to combat oxidative stress and reduce inflammation makes it a candidate for the prevention and treatment of a range of conditions.
Used in Cancer Prevention and Treatment:
In the field of oncology, 2',7-dihydroxy-4'-methoxyisoflavan is utilized as a potential chemopreventive and therapeutic agent. Its structural similarity to estrogen suggests that it may have implications in hormone-related cancers, and ongoing research is exploring its effects on cancer cell growth and proliferation.
Used in Hormone-Related Conditions:
Due to its structural resemblance to estrogen, 2',7-dihydroxy-4'-methoxyisoflavan is used as a potential treatment for hormone-related conditions. It may have applications in managing symptoms associated with hormonal imbalances or conditions such as menopause.
Used in Nutraceutical Industry:
2',7-Dihydroxy-4'-methoxyisoflavan is used as a nutraceutical ingredient for its health-promoting properties. It can be incorporated into dietary supplements and functional foods to support general well-being and potentially reduce the risk of certain diseases.
Used in Cosmetics:
In the cosmetics industry, 2',7-dihydroxy-4'-methoxyisoflavan may be used for its antioxidant properties, potentially offering benefits for skin health and aging, as well as for anti-inflammatory effects that could be beneficial in skincare products.
Overall, 2',7-dihydroxy-4'-methoxyisoflavan's diverse applications reflect its potential as a multifaceted compound with implications in various industries, from healthcare to cosmetics, underscoring the need for continued research to fully understand and harness its benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 56701-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,7,0 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56701-24:
(7*5)+(6*6)+(5*7)+(4*0)+(3*1)+(2*2)+(1*4)=117
117 % 10 = 7
So 56701-24-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H16O4/c1-19-13-4-5-14(15(18)8-13)11-6-10-2-3-12(17)7-16(10)20-9-11/h2-5,7-8,11,17-18H,6,9H2,1H3

56701-24-7SDS

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 vestitol

1.2 Other means of identification

Product number -
Other names 2',7-DIHYDROXY-4'-METHOXYISOFLAVAN

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:56701-24-7 SDS

56701-24-7Downstream Products

56701-24-7Relevant articles and documents

Total syntheses of (±)-vestitol and bolusanthin III using a wittig strategy

Luniwal, Amarjit,Erhardt, Paul W.

, p. 1605 - 1607 (2011/08/03)

An intramolecular Wittig olefination was utilized to -produce the key isoflav-3-ene intermediate needed to prepare (±)-vestitol and bolusanthin III in ca. 30% and 20% respective yields after eight steps. Georg Thieme Verlag Stuttgart ? New York.

o-Quinone methide based approach to isoflavans: application to the total syntheses of equol, 3′-hydroxyequol and vestitol

Gharpure, Santosh J.,Sathiyanarayanan,Jonnalagadda, Prasad

, p. 2974 - 2978 (2008/09/20)

A concise strategy is developed for the synthesis of isoflavans employing a Diels-Alder reaction between o-quinone methides and aryl-substituted enol ethers followed by reductive cleavage of the acetal group. The method is extended towards the total syntheses of equol, 3′-hydroxyequol and vestitol.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 56701-24-7