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(3Z)-3-(4-methoxybenzylidene)dihydrofuran-2(3H)-one, also known as Methyl Benzylidene-γ-Butyrolactone, is a chemical compound with the molecular formula C12H12O3. It is a derivative of furan-2(3H)-one and is known for its sweet, fruity flavor.
Used in Food Industry:
(3Z)-3-(4-methoxybenzylidene)dihydrofuran-2(3H)-one is used as a flavoring agent for its sweet, fruity taste, making it suitable for the production of baked goods, confectionery, and beverages.
Used in Fragrance and Perfume Industry:
(3Z)-3-(4-methoxybenzylidene)dihydrofuran-2(3H)-one is used as a component in the manufacturing of fragrances and perfumes due to its pleasant aroma.
Used in Antioxidant Applications:
(3Z)-3-(4-methoxybenzylidene)dihydrofuran-2(3H)-one exhibits potential antioxidant properties, which can be beneficial in various applications where preservation of products from oxidation is required.
Used in Antimicrobial Applications:
(3Z)-3-(4-methoxybenzylidene)dihydrofuran-2(3H)-one has shown antimicrobial properties, making it a versatile ingredient for use in applications where control of microbial growth is necessary.

1530-62-7

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  • 1530-62-7 Structure

  • Basic information

    1. Product Name: (3Z)-3-(4-methoxybenzylidene)dihydrofuran-2(3H)-one
    2. Synonyms:
    3. CAS NO:1530-62-7
    4. Molecular Formula: C12H12O3
    5. Molecular Weight: 204.2219
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1530-62-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 415.4°C at 760 mmHg
    3. Flash Point: 176.4°C
    4. Appearance: N/A
    5. Density: 1.215g/cm3
    6. Vapor Pressure: 4.13E-07mmHg at 25°C
    7. Refractive Index: 1.6
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (3Z)-3-(4-methoxybenzylidene)dihydrofuran-2(3H)-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3Z)-3-(4-methoxybenzylidene)dihydrofuran-2(3H)-one(1530-62-7)
    12. EPA Substance Registry System: (3Z)-3-(4-methoxybenzylidene)dihydrofuran-2(3H)-one(1530-62-7)

  • 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: 1530-62-7(Hazardous Substances Data)

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1530-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1530-62-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,3 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1530-62:
(6*1)+(5*5)+(4*3)+(3*0)+(2*6)+(1*2)=57
57 % 10 = 7
So 1530-62-7 is a valid CAS Registry Number.

1530-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-3-(4-methoxybenzylidene)dihydrofuran-2(3H)-one

1.2 Other means of identification

Product number -
Other names 3-(4-methoxybenzylidene)indolin-2-one

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:1530-62-7 SDS

1530-62-7Relevant academic research and scientific papers

Novel synthesis of physovenine and physostigmine analogs

Wang,Alluri,Nikogosyan,Decarlo,Monteiro,Mabagos,Feng,White,Bartolini,Andrisano,Zhang,Ganguly

, p. 3046 - 3049 (2016/07/06)

This Letter describes a versatile synthetic approach to prepare physovenine and physostigmine analogs. A series of analogs were synthesized and evaluated for cholinesterase inhibition activities, including human acetylcholinesterase (AChE) and butyrylchol

Cross-metathesis between α-methylene-γ-butyrolactone and olefins: A dramatic additive effect

Moise, Joelle,Arseniyadis, Stellios,Cossy, Janine

, p. 1695 - 1698 (2008/02/02)

Olefin cross-metathesis between α-methylene-γ-butyrolactone and terminal olefins is described. Moderate to excellent yields of α-alkylidene-γ-butyrolactones were obtained with high E-stereoselectivity in the presence of low catalyst loading in refluxing CH 2Cl2. In addition, the use of various additives was found to have a dramatic effect on the efficiency of the cross-metathesis (CM) process by circumventing the formation of the isomerized byproduct.

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