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531-40-8

2-Methoxyphenyl cinnamate, also known as 2-methoxyphenyl 3-phenylprop-2-enoate, is an organic compound with the chemical formula C16H14O3. It is a derivative of cinnamic acid, featuring a cinnamate ester functional group and a 2-methoxyphenyl moiety. 2-methoxyphenyl cinnamate is characterized by its aromatic structure, with a phenyl ring connected to a methoxy group and a cinnamate ester. It is used in various applications, including as a fragrance ingredient and in the synthesis of other organic compounds. The compound is known for its pleasant scent and is often used in the perfume industry. It is also of interest in chemical research due to its potential applications in the development of new materials and pharmaceuticals.

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  • 531-40-8 Structure

  • Basic information

    1. Product Name: 2-methoxyphenyl cinnamate
    2. Synonyms: 2-methoxyphenyl cinnamate;3-Phenylpropenoic acid 2-methoxyphenyl ester;(2-methoxyphenyl) 3-phenylprop-2-enoate;3-phenylacrylic acid (2-methoxyphenyl) ester
    3. CAS NO:531-40-8
    4. Molecular Formula: C16H14O3
    5. Molecular Weight: 254.28056
    6. EINECS: 208-508-6
    7. Product Categories: N/A
    8. Mol File: 531-40-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 413.1°Cat760mmHg
    3. Flash Point: 175.3°C
    4. Appearance: /
    5. Density: 1.156g/cm3
    6. Vapor Pressure: 4.92E-07mmHg at 25°C
    7. Refractive Index: 1.598
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-methoxyphenyl cinnamate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-methoxyphenyl cinnamate(531-40-8)
    12. EPA Substance Registry System: 2-methoxyphenyl cinnamate(531-40-8)

  • 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: 531-40-8(Hazardous Substances Data)

531-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 531-40-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 531-40:
(5*5)+(4*3)+(3*1)+(2*4)+(1*0)=48
48 % 10 = 8
So 531-40-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H14O3/c1-18-14-9-5-6-10-15(14)19-16(17)12-11-13-7-3-2-4-8-13/h2-12H,1H3/b12-11+

531-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methoxyphenyl) 3-phenylprop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid, 3-phenyl-, 2-methoxyphenyl ester

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:531-40-8 SDS

531-40-8Relevant articles and documents

Selective synthesis of 3,4-dihydrocoumarins and chalcones from substituted aryl cinnamic esters

Jeon, Jae-Ho,Yang, Deok-Mo,Jun, Jong-Gab

experimental part, p. 65 - 70 (2011/10/31)

Coumarins are ubiquitous in plant kingdom and have been used as antitumor, antifungals, anticoagulants, insecticides. Chalcones are also widespread in plant kingdom and have been known to possess diverse biological activities; antibacterial, antifungal, antitumor and anti-inflammatory, etc. As they are considered as important natural products, numerous synthetic approaches have been reported up to the present. We devise a new selective method of preparing dihydrocoumarins and chalcones from aryl cinnamates by the selection of reagents. Dihydrocoumarin derivatives were prepared selectively by using intramolecular cyclization catalyzed by p-toluene sulfonic acid. Also, chalcones were prepared by Fries-rearrangement catalyzed by TiCl4. This method can be used for preparing various coumarin & chalcone compounds.

REACTIVITY OF ARYLCINNAMATES IN POLYPHOSPHORIC ACID (PPA): CYCLISATION AND REARRANGEMENT REACTIONS

Dupin, Jean-Francois E.,Chenault, Jacques

, p. 2401 - 2404 (2007/10/02)

In polyphosphoric acid (PPA), various phenyl-substituted cinnamates react to give 4-phenyl-3,4-dihydrocoumarins, flavanones or 3-phenylindanone owing to the nature of the substituents on the phenyl moiety.

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