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15121-89-8

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15121-89-8 Usage

General Description

Ethyl 3-Benzoylacrylate, scientifically known as C12H12O3, is an organic compound that appears as a clear, colorless to pale yellow liquid. It is commonly used in the manufacturing of chemicals, perfumes, paints, pharmaceuticals, and other organic compounds. The substance is radiosensitive and may polymerize exothermically if induced or catalyzed by various materials. While it may present minimal reactivity under normal working conditions, extensive exposure may be toxic and harmful to various body organs. Therefore, when handling this chemical, it is crucial to adhere to safety guidelines and take preventive measures to avoid skin or eye contact, digestion, or inhalation.

Check Digit Verification of cas no

The CAS Registry Mumber 15121-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,2 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15121-89:
(7*1)+(6*5)+(5*1)+(4*2)+(3*1)+(2*8)+(1*9)=78
78 % 10 = 8
So 15121-89-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O3/c1-2-15-12(14)9-8-11(13)10-6-4-3-5-7-10/h3-9H,2H2,1H3

15121-89-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 3-BENZOYLACRYLATE

1.2 Other means of identification

Product number -
Other names ethyl benzo<b>thiophen-3-ylacetate

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:15121-89-8 SDS

15121-89-8Relevant articles and documents

Rhodium-Catalysed Redox Isomerization of Hydroxy Alkynes to Trans Keto and Hydroxy Vinyl Esters. A Short and Stereoselective Synthesis of Dipeptide Isosters

Saiah, M. K. Eddine,Pellicciari, Roberto

, p. 4497 - 4500 (1995)

Tris(triphenylphosphine)Rhodium(I) Chloride in the presence trialkyl phosphine catalyses the isomerization of hydroxy alkynes to unsaturated trans keto and hydroxy esters depending on the nature of the phosphine.Dipeptide isosters were obtained in an efficient manner by the application of this methodology.

Copper-Catalyzed N-O Cleavage of α,β-Unsaturated Ketoxime Acetates toward Structurally Diverse Pyridines

Ding, Xiaojuan,Duan, Jindian,Fang, Zheng,Guo, Kai,Li, Zhenjiang,Mao, Yiyang,Rong, Binsen,Xu, Gaochen,Zhang, Lei,Zhu, Ning

, p. 2532 - 2542 (2020/03/13)

The copper-catalyzed [4 + 2] annulation of α,β-unsaturated ketoxime acetates with 1,3-dicarbonyl compounds for the synthesis of three classes of structurally diverse pyridines has been developed. This method employs 1,3-dicarbonyl compounds as C2 synthons and enables the synthesis of multifunctionalized pyridines with diverse electron-withdrawing groups in moderate to good yields. The mechanistic investigation suggests that the reactions proceed through an ionic pathway.

Chiral Hydroxytetraphenylene-Catalyzed Asymmetric Conjugate Addition of Boronic Acids to Enones

Chai, Guo-Li,Sun, A-Qiang,Zhai, Dong,Wang, Juan,Deng, Wei-Qiao,Wong, Henry N.C.,Chang, Junbiao

supporting information, p. 5040 - 5045 (2019/07/03)

(S)-2,15-Br2-DHTP-catalyzed asymmetric conjugate addition of boronic acids to β-trifluoromethyl α,β-unsaturated ketones and enones was studied. The reaction afforded the corresponding Michael addition products in moderate to high yields with excellent enantioselectivities (up to 99:1 er). This catalytic system features mild reaction conditions, high efficiency, and tolerance to heteroarylboronic acids.

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