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5292-53-5

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5292-53-5 Usage

Uses

Diethyl benzylidenemalonate is used as a pharmaceutical intermediate. It is also involved in the Conjugate addition of cyanide ion to arylidenemalonic esters provides a useful route to arylsuccinic acids.

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 3, p. 377, 1955Tetrahedron Letters, 33, p. 7535, 1992 DOI: 10.1016/S0040-4039(00)60817-1

Check Digit Verification of cas no

The CAS Registry Mumber 5292-53-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,9 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5292-53:
(6*5)+(5*2)+(4*9)+(3*2)+(2*5)+(1*3)=95
95 % 10 = 5
So 5292-53-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H16O4/c1-3-17-13(15)12(14(16)18-4-2)10-11-8-6-5-7-9-11/h5-10H,3-4H2,1-2H3

5292-53-5 Well-known Company Product Price

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  • Alfa Aesar

  • (L00561)  Diethyl benzylidenemalonate, 98%   

  • 5292-53-5

  • 25g

  • 311.0CNY

  • Detail
  • Alfa Aesar

  • (L00561)  Diethyl benzylidenemalonate, 98%   

  • 5292-53-5

  • 100g

  • 776.0CNY

  • Detail

5292-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name DIETHYL BENZYLIDENEMALONATE

1.2 Other means of identification

Product number -
Other names Benzylidenemalonic Acid Diethyl 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:5292-53-5 SDS

5292-53-5Relevant articles and documents

Bifunctional acid-base ionic liquid organocatalysts with a controlled distance between acid and base sites

Boronat, Mercedes,Climent, Maria J.,Corma, Avelino,Iborra, Sara,Monton, Raquel,Sabater, Maria J.

, p. 1221 - 1231 (2010)

Bifunctional acid-base ionic liquid organocatalysts with different distances between the two sites have been synthesised, and their activity for the Knoevenagel condensation has been tested. As has been found to be the case with enzymes, the distance betw

Synthesis, characterization, and catalytic activity of ionic liquids based on biosources

Moriel,García-Suárez,Martínez,García,Montes-Morán,Calvino-Casilda,Ba?ares

, p. 4877 - 4881 (2010)

New room-temperature ionic liquids were synthesized from natural and easily available feedstocks (choline hydroxide and amino acids) following an economical and green route in which the only by-product was water. They were successfully applied as catalyst

Mg/Al-CO3 layered double hydroxide nanorings

Yang, Miaosen,Liu, Junfeng,Chang, Zheng,Williams, Gareth R.,O'Hare, Dermot,Zheng, Xuehan,Sun, Xiaoming,Duan, Xue

, p. 14741 - 14746 (2011)

Mg/Al-CO3 Layered Double Hydroxide (LDH) nanorings with a 750 nm exterior diameter and 250 nm interior diameter were synthesized in an organic/water solvent system via a urea hydrolysis method, using Mg 10(OH)18Cl2/s

Alkaline carbons as effective catalysts for the microwave-assisted synthesis of N-substituted-gamma-lactams

Calvino-Casilda,Martín-Aranda,López-Peinado

, p. 73 - 81 (2011)

The selective construction of new CC or Cheteroatom bonds is frequently the fundamental step in the synthesis of derivatives with high added value. In particular, molecules with CN bonds are of great interest due to their widespread use and intrinsic impo

Highly Active Bisamino Functionalized Zr(IV)-UiO-67 Metal-Organic Framework for Cascade Catalysis

Das, Aniruddha,Anbu, Nagaraj,Mostakim,Dhakshinamoorthy, Amarajothi,Biswas, Shyam

supporting information, p. 2830 - 2834 (2020/07/04)

This work reports the synthesis and characterization of Zr(IV)-based UiO-67-(NH2)2 (called 1) metal-organic framework. Activated 1 (named 1') was shown to be an efficient tandem catalyst in the conversion of benzaldehydedimethyl acet

Johnson-Corey-Chaykovsky fluorocyclopropanation of double activated alkenes: Scope and limitations

Kazia, Armands,Melngaile, Renate,Mishnev, Anatoly,Veliks, Janis

supporting information, p. 1384 - 1388 (2020/03/03)

Johnson-Corey-Chaykovsky fluorocyclopropanation of double activated alkenes utilizing S-monofluoromethyl-S-phenyl-2,3,4,5-tetramethylphenylsulfonium tetrafluoroborate is an efficient approach to obtain a range of monofluorocyclopropane derivatives. So far, fluoromethylsulfonium salts have displayed the broadest scope for direct fluoromethylene transfer. In contrast to more commonly used fluorohalomethanes or freon derivatives, diarylfluoromethylsulfonium salts are bench stable, easy-to use reagents useful for the direct transfer of a fluoromethylene group to alkenes giving access to the challenging products-fluorocyclopropane derivatives. Interplay between the reactivity of the starting materials and stability of the fluorocyclopropanes formed determines the outcome of the process.

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