beta-Alanine, N-carbamoyl-N-(3,4-dichlorobenzyl)-

Base Information

Chemical Name:beta-Alanine, N-carbamoyl-N-(3,4-dichlorobenzyl)-
CAS No.:4010-58-6
Molecular Formula:C11H12Cl2N2O3
Molecular Weight:291.1306
Hs Code.:
DSSTox Substance ID:DTXSID00193143
Wikidata:Q83065861

Synonyms:beta-Alanine, N-carbamoyl-N-(3,4-dichlorobenzyl)-;4010-58-6;N-Carbamoyl-N-(3,4-dichlorobenzyl)-beta-alanine;C11H12Cl2N2O3;DTXSID00193143

Suppliers and Price of beta-Alanine, N-carbamoyl-N-(3,4-dichlorobenzyl)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of beta-Alanine, N-carbamoyl-N-(3,4-dichlorobenzyl)-

Chemical Property:

Vapor Pressure:1.75E-10mmHg at 25°C
Boiling Point:491.7°Cat760mmHg
Flash Point:251.2°C
Density:1.467g/cm³
XLogP3:1.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:290.0224976
Heavy Atom Count:18
Complexity:315

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=C(C=C1CN(CCC(=O)O)C(=O)N)Cl)Cl

Technology Process of beta-Alanine, N-carbamoyl-N-(3,4-dichlorobenzyl)-

There total 4 articles about beta-Alanine, N-carbamoyl-N-(3,4-dichlorobenzyl)- 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: 73.0%

: 590-28-3
potassium cyanate

: 76479-09-9
3-(3,4-dichlorobenzylamino)propanoic acid

: 4010-58-6
3-<1-(3,4-dichlorobenzyl)-1-ureido>proppanoic acid

Guidance literature:: With acetic acid; In water; for 19h; Ambient temperature;
DOI:10.1002/jps.2600691022

Reference yield:

: 102-49-8
3,4-dichlorobenzyl amine

: 4010-58-6
3-<1-(3,4-dichlorobenzyl)-1-ureido>proppanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate, NaI / ethanol / 18 h / Heating

2: 76 percent / KOH / H₂O / 3 h / Heating

3: 73 percent / acetic acid / H₂O / 19 h / Ambient temperature

With potassium hydroxide; potassium carbonate; acetic acid; sodium iodide; In ethanol; water;
DOI:10.1002/jps.2600691022

Reference yield:

: 76479-08-8
ethyl 3-(3,4-dichlorobenzylamino)propanoate

: 4010-58-6
3-<1-(3,4-dichlorobenzyl)-1-ureido>proppanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / KOH / H₂O / 3 h / Heating

2: 73 percent / acetic acid / H₂O / 19 h / Ambient temperature

With potassium hydroxide; acetic acid; In water;
DOI:10.1002/jps.2600691022