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54494-74-5

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54494-74-5 Usage

General Description

DIMETHYL 2-ANILINOBUT-2-ENEDIOATE is a chemical compound with the molecular formula C14H15NO4. It is also known as Methyl 2-(Dimethylamino)itaconate, and it is a yellow to brown crystalline powder. DIMETHYL 2-ANILINOBUT-2-ENEDIOATE is commonly used as an intermediate in the synthesis of other organic compounds, and it is also used in the manufacturing of pharmaceuticals and agrochemicals. DIMETHYL 2-ANILINOBUT-2-ENEDIOATE is also used as a dye intermediate and as a reagent in organic synthesis. It has a wide range of applications in various industries due to its versatile chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 54494-74-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,9 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54494-74:
(7*5)+(6*4)+(5*4)+(4*9)+(3*4)+(2*7)+(1*4)=145
145 % 10 = 5
So 54494-74-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO4/c1-16-11(14)8-10(12(15)17-2)13-9-6-4-3-5-7-9/h3-8,13H,1-2H3/b10-8+

54494-74-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 1-(N-phenylamino)-ethene-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names DIMETHYL2-(PHENYLAMINO)-2-BUTENEDIOATE

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:54494-74-5 SDS

54494-74-5Relevant articles and documents

Synthesis, crystal structure and dft studies of polyfunctionalized alkenes: A transition metal-free c(sp2)-h sulfenylation of electron deficient alkyne

Khurana, J. M.,Kumar, Parvin,Saroha, Mohit,Sindhu, Jayant

, (2020/08/24)

An efficient, novel and transition metal-free protocol has been developed for the synthesis of polyfunctionalized aminothioalkenes via direct C[sbnd]H sulfenylation of in situ generated enamines. The reaction was performed using a catalytic amount of inex

One-pot synthesis of 2,4-disubstituted quinolines via silver-catalyzed three-component cascade annulation of amines, alkyne esters and terminal alkynes

Li, Yunlan,Zhang, Qiurui,Xu, Xuefeng,Zhang, Xu,Yang, Yurong,Yi, Wei

supporting information, p. 965 - 970 (2019/03/13)

Described herein is a new and general method for one-pot synthesis of 2,4-disubstituted quinolines via silver-catalyzed [3 + 1 + 2] annulation of simple amines, alkyne esters and terminal alkynes. The versatile transformation might initiate with the facil

Stereoselective Aminoiodination of Activated Alkynes with Organoiodine(III) Reagents and Amines via Multiple-Site Functionalization: Access to Iodinated Enamines and N-Aryl Indoles

Arepally, Sagar,Chamuah, Ajoy,Katta, Narenderreddy,Sharada, Duddu S.

supporting information, p. 1542 - 1547 (2019/02/03)

A stereoselective aminoiodination of activated alkynes with PhI(OAc)2 and amines via multiple-site functionalization to afford (Z)diethyl 2-(diphenylamino)-3-iodomaleate derivatives with superior yields has been described. The key feature of th

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