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4'-O-METHYLDAVIDIGENIN is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 65428-04-8 Structure
  • Basic information

    1. Product Name: 4'-O-METHYLDAVIDIGENIN
    2. Synonyms: 4'-O-METHYLDAVIDIGENIN
    3. CAS NO:65428-04-8
    4. Molecular Formula: C16H16O4
    5. Molecular Weight: 272.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 65428-04-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 503.4°C at 760 mmHg
    3. Flash Point: 189.6°C
    4. Appearance: /
    5. Density: 1.243g/cm3
    6. Vapor Pressure: 9.37E-11mmHg at 25°C
    7. Refractive Index: 1.609
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4'-O-METHYLDAVIDIGENIN(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4'-O-METHYLDAVIDIGENIN(65428-04-8)
    12. EPA Substance Registry System: 4'-O-METHYLDAVIDIGENIN(65428-04-8)
  • 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: 65428-04-8(Hazardous Substances Data)

65428-04-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65428-04-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,2 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65428-04:
(7*6)+(6*5)+(5*4)+(4*2)+(3*8)+(2*0)+(1*4)=128
128 % 10 = 8
So 65428-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H16O4/c1-20-13-7-8-14(16(19)10-13)15(18)9-4-11-2-5-12(17)6-3-11/h2-3,5-8,10,17,19H,4,9H2,1H3

65428-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-hydroxy-4-methoxyphenyl)-3-(4-hydroxyphenyl)propan-1-one

1.2 Other means of identification

Product number -
Other names 4'-O-Methyldavidigenin

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:65428-04-8 SDS

65428-04-8Downstream Products

65428-04-8Relevant articles and documents

COMPOSITIONS AND METHODS OF TREATING UPS-ASSOCIATED DISEASES

-

, (2022/01/24)

The present invention relates to methods for treating a disease characterized by aberrations in the ubiquitin/proteasome system (UPS).

NOTCH INHIBITORS FOR USE IN THE TREATMENT OF T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA

-

Page/Page column 26; 31, (2018/07/29)

Compounds of formula (I) in the capacity of compounds with anti-tumor activity for the treatment of T-cell acute lymphoblastic leukemia (T-ALL).

Synthesis, anticancer, structural, and computational docking studies of 3-benzylchroman-4-one derivatives

Simon, Lalitha,Abdul Salam, Abdul Ajees,Madan Kumar,Shilpa,Srinivasan,Byrappa

, p. 5284 - 5290 (2017/10/30)

A series of 3-Benzylchroman-4-ones were synthesized and screened for anticancer activity by MTT assay. The compounds were evaluated against two cancerous cell lines BT549 (human breast carcinoma), HeLa (human cervical carcinoma), and one noncancerous cell

Microbial Transformations of 7-Methoxyflavanone

Kostrzewa-Suslow, Edyta,Janeczko, Tomasz

, p. 14810 - 14820 (2013/02/26)

Microbial transformations of racemic 7-methoxyflavanone using strains of the genus Aspergillus (A. niger KB, A. ochraceus 456) and the strain Penicillium chermesinum 113 were described. The strain A. niger KB catalysed carbonyl group reduction, leading to (±)-2,4-cis-7-methoxyflavan-4-ol. Biotransformation with the help of A. ochraceus 456 gave two products: (+)-2,4-trans-7-methoxyflavan-4-ol and 4'-hydroxy-7-methoxyflavone. Transformation by means of P. chermesinum 113 resulted in a dihydrochalcone product, 4,2'-dihydroxy-4'-methoxydihydrochalcone. DPPH scavenging activity test proved that all the biotransformations products have higher antioxidant activity that the substrate.

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