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METHYL 3-(2-METHOXYPHENYL)-2-PHENYLACRYLATE, a chemical compound with the molecular formula C17H16O3, is a member of the acrylate family. It is characterized by a 3-(2-methoxyphenyl)-2-phenylacrylate structure and is recognized for its versatility and value as a chemical intermediate. METHYL 3-(2-METHOXYPHENYL)-2-PHENYLACRYLATE is commonly utilized in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds, as well as in the production of specialty chemicals and materials. Its potential applications extend to the field of organic electronics and materials science, making it a promising candidate for various industrial and research applications.

42307-45-9

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42307-45-9 Usage

Uses

Used in Pharmaceutical Synthesis:
METHYL 3-(2-METHOXYPHENYL)-2-PHENYLACRYLATE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with improved therapeutic properties.
Used in Agrochemical Production:
In the agrochemical industry, METHYL 3-(2-METHOXYPHENYL)-2-PHENYLACRYLATE is used as a building block for the creation of new agrochemicals, enhancing crop protection and yield.
Used in Organic Compounds Synthesis:
METHYL 3-(2-METHOXYPHENYL)-2-PHENYLACRYLATE is utilized as a versatile component in the synthesis of various organic compounds, contributing to the advancement of organic chemistry.
Used in Specialty Chemicals and Materials Production:
METHYL 3-(2-METHOXYPHENYL)-2-PHENYLACRYLATE is used as a crucial ingredient in the production of specialty chemicals and materials, where its unique structure imparts specific properties to the final products.
Used in Organic Electronics and Materials Science:
METHYL 3-(2-METHOXYPHENYL)-2-PHENYLACRYLATE is employed in the field of organic electronics and materials science for its potential to contribute to the development of innovative electronic devices and materials with enhanced performance characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 42307-45-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,3,0 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 42307-45:
(7*4)+(6*2)+(5*3)+(4*0)+(3*7)+(2*4)+(1*5)=89
89 % 10 = 9
So 42307-45-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H16O3/c1-19-16-11-7-6-10-14(16)12-15(17(18)20-2)13-8-4-3-5-9-13/h3-12H,1-2H3/b15-12+

42307-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-(2-methoxyphenyl)-2-phenylacrylate

1.2 Other means of identification

Product number -
Other names methyl (E)-3-(2-methoxyphenyl)-2-phenylacrylate

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:42307-45-9 SDS

42307-45-9Relevant academic research and scientific papers

Palladium-catalyzed cross coupling reaction of benzyl bromides with diazoesters for stereoselective synthesis of (E)-α,β-diarylacrylates

Yu, Wing-Yiu,Tsoi, Yuk-Tai,Zhou, Zhongyuan,Chan, Albert S. C.

supporting information; experimental part, p. 469 - 472 (2009/07/11)

(Chemical Equation Presented) A Pd-catalyzed cross-coupling reaction of benzyl bromides with α-aryldiazoesters is described, and E-α,β-diarylacrylates were obtained in good yields and excellent E-to-Z selectivity (>20:1).

Synthesis of E- and Z-o-methoxy-substituted 2,3-diphenyl propenoic acids and its methyl esters

Felfoeldi, Karoly,Sutyinszky, Maria,Nagy, Nora,Palinko, Istvan

, p. 1543 - 1553 (2007/10/03)

A series of stereoisomeric o-methoxy-substituted 2,3-diphenyl propenoic acids and their methyl esters have been synthesized. The E isomers were prepared by a modified Perkin condensation (substituted benzaldehyde, phenylacetic acid, Et3N/acetic anhydride). The difficult to access Z isomers were obtained conveniently in good yields when the appropriate coumarin derivatives were allowed to react with KOH and CH3I in DMSO.

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