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N,N'-Diacetylethylethenediamine, also known as DAE, is an organic compound with the chemical formula C6H12N2O2. It is a colorless, viscous liquid that is soluble in water and serves as an important intermediate in the synthesis of various chemicals, including dyes, pharmaceuticals, and agrochemicals. DAE is produced through the reaction of ethylenediamine with acetic anhydride, resulting in the formation of a symmetrical urea derivative. Due to its reactivity and versatility, DAE is widely used in the chemical industry for the preparation of various products, such as disperse dyes for polyester fibers and other specialty chemicals.

5335-91-1

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5335-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5335-91-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5335-91:
(6*5)+(5*3)+(4*3)+(3*5)+(2*9)+(1*1)=91
91 % 10 = 1
So 5335-91-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H12N2O2/c1-4(7-5(2)9)8-6(3)10/h4H,1-3H3,(H,7,9)(H,8,10)

5335-91-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1-acetamidoethyl)acetamide

1.2 Other means of identification

Product number -
Other names 1,1-Bis-acetylamino-aethan

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:5335-91-1 SDS

5335-91-1Relevant academic research and scientific papers

Reactions of ethylidene diacetate: Formation of N-vinylamide precursors ethylidene bisacetamide and ethylidene bisformamide

Rabasco, John J.,Waller, Francis J.

, p. 4953 - 4956 (2007/10/03)

Ethylidene diacetate (EDA) reacts with formamide or acetamide under stoichiometric base or catalytic Lewis acid conditions to afford the corresponding ethylidene bisamides and N-vinylamides. Sn(OAc)2 afforded an overall 82.6% selectivity to the desired acetamide derivatives. Sn(OAc)2 and Zn(OAc)2 facilitate amide attack at the tertiary carbon of EDA.

The Synthesis of 1-Aminoalkylphosphonic Acids. A Revised Mechanism of the Reaction of Phosphorus Trichloride, Amides and Aldehydes or Ketones in Acetic Acid (Oleksyszyn Reaction)

Soroka, Miroslaw

, p. 331 - 334 (2007/10/02)

The mechanism of the amidoalkylation of trivalent phosphorus compounds in acetic acid has been reinvestigated.Evidence is presented that 1-(acylamino)alkyl acetates 5 and not N,N'-alkylidenebisamides 2 are the intermediates in this reaction.Supporting literature analogies are discussed.This paper also describes a convenient procedure for the preparation of crude (acylamino)alkyl alkanoates 5, which are excellent amidoalkylating agents.The usefulness of these reagents is demonstrated by a simple two-step "one pot" synthesis of 1-aminoalkylphosphinic acids 1.

REACTION OF THE AMIDES OF MONOCARBOXYLIC ACIDS WITH VINYL ALKYL ETHERS AND THE STRUCTURE OF THE ADDITION PRODUCTS

Voronkov, M. G.,Keiko, N. A.,Kuznetsova, T. A.,Frolov, Yu. L.,Kalikhman, I. D.,Chuvashev, Yu. A.

, p. 1738 - 1741 (2007/10/02)

The reaction of vinyl alkyl ethers with the amides of monocarboxylic acids leads to the formation of 1,1-di(acylamino)ethanes.

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