Acetic acid, bis[(1-oxo-2-propenyl)amino]-

Base Information

• Chemical Name: Acetic acid, bis[(1-oxo-2-propenyl)amino]-
• CAS No.: 4387-85-3
• Deprecated CAS: 134337-66-9
• Molecular Formula: C8H10 N2 O4
• Molecular Weight: 198.178
• Hs Code.: 2924199090
• European Community (EC) Number: 224-500-5
• DSSTox Substance ID: DTXSID00884069
• Nikkaji Number: J205.764F
• Wikidata: Q82862820
• Mol file: 4387-85-3.mol

Synonyms:4387-85-3;Acetic acid, bis[(1-oxo-2-propenyl)amino]-;2,2-Bis(acrylamido)acetic acid;EINECS 224-500-5;Acetic acid, bis((1-oxo-2-propenyl)amino)-;Acetic acid, 2,2-bis((1-oxo-2-propen-1-yl)amino)-;Bis((1-oxoallyl)amino)acetic acid;BIS[(1-OXOALLYL)AMINO]ACETIC ACID;Acetic acid, 2,2-bis[(1-oxo-2-propen-1-yl)amino]-;bisacrylamidoacetic acid;SCHEMBL196271;Bis(acryloylamino)acetic acid #;DTXSID00884069;2,2-bis(acryloylamino)acetic acid;2,2-Bis-(prop-2-enoylamino)acetic acid;FT-0627070;2-(Ethoxycarbonyl)Ethyltriphenylphosphoniumbromi

Chemical Property of Acetic acid, bis[(1-oxo-2-propenyl)amino]-

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Boiling Point: 572.051°C at 760 mmHg
• Flash Point: 299.766°C
• PSA: 102.48000
• LogP: 0.68210
• XLogP3: -0.2
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 198.06405680
• Heavy Atom Count: 14
• Complexity: 263

Purity/Quality:

98%Min ^*data from raw suppliers

BIS-[(1-OXO-2-PROPENYL)AMINO]ACETIC ACID 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C=CC(=O)NC(C(=O)O)NC(=O)C=C

Technology Process of Acetic acid, bis[(1-oxo-2-propenyl)amino]-

There total 2 articles about Acetic acid, bis[(1-oxo-2-propenyl)amino]- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

2-acrylamidoglycolic acid (6737-24-2) + acrylonitrile (107-13-1,25014-41-9) → N,N'-bis(acrylamido)acetic acid (4387-85-3)

Guidance literature:

With sulfuric acid;

Reference yield:

→ N,N'-bis(acrylamido)acetic acid (4387-85-3)

Guidance literature:

Acrylamid, OCHCO2H;

upstream raw materials:

2-acrylamidoglycolic acid

acrylonitrile

Refernces