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CAS

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40110-95-0

3-[4-(benzyloxy)phenyl]-1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)prop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 40110-95-0 Structure

  • Basic information

    1. Product Name: 3-[4-(benzyloxy)phenyl]-1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)prop-2-en-1-one
    2. Synonyms:
    3. CAS NO:40110-95-0
    4. Molecular Formula: C26H26O7
    5. Molecular Weight: 450.4804
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 40110-95-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 663.1°C at 760 mmHg
    3. Flash Point: 223.9°C
    4. Appearance: N/A
    5. Density: 1.22g/cm3
    6. Vapor Pressure: 3.42E-18mmHg at 25°C
    7. Refractive Index: 1.603
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-[4-(benzyloxy)phenyl]-1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)prop-2-en-1-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-[4-(benzyloxy)phenyl]-1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)prop-2-en-1-one(40110-95-0)
    12. EPA Substance Registry System: 3-[4-(benzyloxy)phenyl]-1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)prop-2-en-1-one(40110-95-0)

  • 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: 40110-95-0(Hazardous Substances Data)

40110-95-0 Usage

General Description

3-[4-(benzyloxy)phenyl]-1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)prop-2-en-1-one is a chemical compound that belongs to the class of chalcones, which are compounds with a 1,3-diphenyl-2-propen-1-one skeleton. This particular chalcone contains a benzyl group and a hydroxy tetramethoxyphenyl group, giving it unique properties and potential applications. Chalcones are known for their diverse pharmacological activities, including antioxidant, anti-inflammatory, anticancer, antidiabetic, and antimicrobial properties, making 3-[4-(benzyloxy)phenyl]-1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)prop-2-en-1-one of interest for further study in the fields of pharmaceuticals and medicinal chemistry. Overall, 3-[4-(benzyloxy)phenyl]-1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)prop-2-en-1-one is a compound with potential therapeutic benefits and is worth further investigation for its pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 40110-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,1 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40110-95:
(7*4)+(6*0)+(5*1)+(4*1)+(3*0)+(2*9)+(1*5)=60
60 % 10 = 0
So 40110-95-0 is a valid CAS Registry Number.

40110-95-0SDS

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 1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)-3-(4-phenylmethoxyphenyl)prop-2-en-1-one

1.2 Other means of identification

Product number -
Other names Phenol,2-[(dimethylamino)methyl]-4-(phenylmethoxy)

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:40110-95-0 SDS

40110-95-0Relevant articles and documents

Biotransformation of polymethoxylated flavonoids: Access to their 4′-O-demethylated metabolites

Buisson, Didier,Quintin, Jerome,Lewin, Guy

, p. 1035 - 1038 (2008/02/13)

Regioselective O-demethylation of the flavones tangeretin (1) and 3-hydroxytangeretin (6) into their 4′-O-demethylated metabolites was performed by using an Aspergillus niger strain. This method serves as a straightforward alternative to multistep synthes

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