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5396-71-4

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5396-71-4 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 68, p. 376, 1946 DOI: 10.1021/ja01207a009

Check Digit Verification of cas no

The CAS Registry Mumber 5396-71-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5396-71:
(6*5)+(5*3)+(4*9)+(3*6)+(2*7)+(1*1)=114
114 % 10 = 4
So 5396-71-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO4/c1-2-16-11(13)7-6-9-4-3-5-10(8-9)12(14)15/h3-8H,2H2,1H3/b7-6+

5396-71-4 Well-known Company Product Price

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  • Alfa Aesar

  • (A12995)  Ethyl 3-nitrocinnamate, 98%   

  • 5396-71-4

  • 5g

  • 398.0CNY

  • Detail
  • Alfa Aesar

  • (A12995)  Ethyl 3-nitrocinnamate, 98%   

  • 5396-71-4

  • 25g

  • 1509.0CNY

  • Detail

5396-71-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 3-(3-nitrophenyl)acrylate

1.2 Other means of identification

Product number -
Other names Ethyl 3-nitrocinnamate

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:5396-71-4 SDS

5396-71-4Relevant articles and documents

Pd/Cu-Free Cobalt-Catalyzed Suzuki and Heck Using Green Bio-Magnetic Hybrid and DFT-Based Theoretical Study

Hajipour, Abdol R.,Khorsandi, Zahra,Ahmadi, Mehnoosh,Jouypazadeh, Hamidreza,Mohammadi, Bahareh,Farrokhpour, Hossein

, p. 2842 - 2850 (2021/02/01)

Abstract: Several highly efficient and magnetically recyclable cobalt catalytic systems were prepared using magnetic chitosan and some safe and available organic compounds (Co-ligand@MNPs/Ch). The structure of these nanocomposites was confirmed by various physicochemical techniques such as FT-IR, XRD, TGA, VSM, TEM, SEM, CHNS and ICP-OES. These nano composites exhibit remarkable catalytic efficiency for Suzuki and Heck cross-coupling reactions in mild and green reaction conditions. The facile accessibility of starting materials, possible performance in air and eco-friendly conditions are merits of our catalysts. In addition, to describe and go insight to role and effect of ligands present in these catalysts, electrostatic interactions, density functional theory (DFT) model in molecular method were employed. Graphic Abstract: [Figure not available: see fulltext.]

Fabrication of Pd/CuFe2O4 hybrid nanowires: A heterogeneous catalyst for Heck couplings

Lakshminarayana,Mahendar,Ghosal,Sreedhar,Satyanarayana,Subrahmanyam, Ch.

, p. 1646 - 1654 (2018/02/09)

The development of environmentally benign transformations is indispensable in organic synthesis. Herein, a hybrid heterogeneous catalyst, palladium(0) on copper ferrite nanowires, has been synthesized, characterized, and for the first time, employed in the Jeffrey Heck reaction between iodoarenes and allylic alcohols, and good to excellent yields have been obtained. In addition, the catalyst was found to be suitable for the usual Heck coupling. The nanocatalyst was recovered and reused up-to multiple runs without any noticeable loss of its catalytic activity.

N, N-disubstituted benzo-nitrogen heterocycles-2-amine compound and use thereof

-

Paragraph 0089-0092, (2016/10/09)

The invention mainly relates to an N,N-double substituted benzoazacyclo-2-amide compound and an application thereof. The N,N-double substituted benzoazacyclo-2-amide compound is a compound shown as formula I or a salt formed by a medical acid or alkali. The compound provided by the invention has strong inhibition activity on RhoA protease which is tightly related with cardiovascular and cerebrovascular diseases. The compound provided by the invention is hopeful to be developed into a RhoA protease small-molecule inhibitor type cardiovascular and cerebrovascular disease treatment medicine.

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