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4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-2,3-dihydro-5-hydroxy-7-methoxy-, (S)is a chemical compound belonging to the benzopyran class. It features a benzopyran ring with a 2-(3,4-dimethoxyphenyl) group at the 2-position and a 5-hydroxy-7-methoxy group at the 3-position. 4H-1-Benzopyran-4-one,
2-(3,4-dimethoxyphenyl)-2,3-dihydro-5-hydroxy-7-methoxy-, (S)exists in the (S)-enantiomeric form, which may confer unique biological activities and pharmacological properties due to its distinct molecular structure. This makes it a promising candidate for research and development in medicinal chemistry and pharmaceuticals.

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  • 70987-96-1 Structure
  • Basic information

    1. Product Name: 4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-2,3-dihydro-5-hydroxy-7-methoxy-, (S)-
    2. Synonyms:
    3. CAS NO:70987-96-1
    4. Molecular Formula: C18H18O6
    5. Molecular Weight: 330.337
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 70987-96-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-2,3-dihydro-5-hydroxy-7-methoxy-, (S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-2,3-dihydro-5-hydroxy-7-methoxy-, (S)-(70987-96-1)
    11. EPA Substance Registry System: 4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-2,3-dihydro-5-hydroxy-7-methoxy-, (S)-(70987-96-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 70987-96-1(Hazardous Substances Data)

70987-96-1 Usage

Uses

Used in Pharmaceutical Industry:
4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-2,3-dihydro-5-hydroxy-7-methoxy-, (S)is used as a pharmaceutical compound for its potential biological activities and pharmacological properties. Its unique molecular structure allows it to interact with various biological targets, making it a candidate for the development of new drugs and therapies.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-2,3-dihydro-5-hydroxy-7-methoxy-, (S)is used as a research compound to explore its potential applications in drug discovery. Its unique structure and properties can be further investigated and optimized to develop new therapeutic agents with improved efficacy and selectivity.
Used in Drug Delivery Systems:
4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-2,3-dihydro-5-hydroxy-7-methoxy-, (S)can be used in drug delivery systems to improve the bioavailability and therapeutic outcomes of other drugs. Its unique structure and properties can be utilized to design novel drug delivery systems, such as nanoparticles or liposomes, to enhance the delivery and targeting of therapeutic agents.
Used in Natural Product Research:
As a chemical compound derived from natural sources, 4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-2,3-dihydro-5-hydroxy-7-methoxy-, (S)can be used in natural product research to study its potential as a bioactive compound. Its unique structure and properties can be further explored to understand its role in various biological processes and its potential as a lead compound for the development of new drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 70987-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,9,8 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70987-96:
(7*7)+(6*0)+(5*9)+(4*8)+(3*7)+(2*9)+(1*6)=171
171 % 10 = 1
So 70987-96-1 is a valid CAS Registry Number.

70987-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-5-hydroxy-3',4',7-trimethoxyflavanone

1.2 Other means of identification

Product number -
Other names 5-hydroxy-7,3',4'-trimethoxyflavanone

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:70987-96-1 SDS

70987-96-1Downstream Products

70987-96-1Relevant articles and documents

Structure-activity relationships of biflavonoids for β-secretase (BACE-1) inhibitory activity

Sasaki, Hiroaki,Kitoh, Yuki,Miki, Kazuhiko,Kinoshita, Kaoru,Koyama, Kiyotaka,Kaneda, Miyuki,Takahashi, Kunio

, p. 2749 - 2756 (2013/01/15)

Bioactive natural products are useful sources of new pharmaceutics. Their analogues are also important for evaluating structure-activity relationships. In this study the structure-activity relationships of 2,3-dihydro-6-methylginketin (1) for BACE-1 inhibitory activity were studied. Biflavonoids consisting of flavanone and flavone, and also the presence of a methoxy group at the C-4' position, were found to be important for strong activity. 2,3-Dihydro-6- methylbilobetin (2) showed strong activity with an IC50 value of 0.56 μM.

Photochemical Deoxygenation of an α-Ketol: The Dihydroflavonol-Flavanone Conversion

Westhuizen, Jan H. van der,Ferreira, Daneel,Roux, David G.

, p. 1003 - 1006 (2007/10/02)

Irradiation of optically pure 2,3-trans-3-hydroxyflavanones in anhydrous ethyl acetate leads directly to free phenolic flavanone analogues with complete retention of configuration at C(2).Similarly their methyl ethers give the corresponding flavanones and flavones.The reaction represents the photochemical equivalent of a reduction under Clemmensen conditions.

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