Methyl 4-(2,4-diaminophenyl)butanoate

Base Information

Chemical Name:Methyl 4-(2,4-diaminophenyl)butanoate
CAS No.:113849-32-4
Molecular Formula:C11H16N2O2
Molecular Weight:208.26
Hs Code.:
DSSTox Substance ID:DTXSID00554977
Wikidata:Q82436178
Mol file:113849-32-4.mol

Synonyms:Methyl 4-(2,4-diaminophenyl)butanoate;113849-32-4;DTXSID00554977

Suppliers and Price of Methyl 4-(2,4-diaminophenyl)butanoate

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 1 raw suppliers

Chemical Property of Methyl 4-(2,4-diaminophenyl)butanoate

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:208.121177757
Heavy Atom Count:15
Complexity:209

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC(=O)CCCC1=C(C=C(C=C1)N)N

Technology Process of Methyl 4-(2,4-diaminophenyl)butanoate

There total 2 articles about Methyl 4-(2,4-diaminophenyl)butanoate 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: 65.0%

: 22824-20-0
4(2-nitrophenyl)butanoic acid methyl ester

: 113849-32-4
4-(2,4-Diamino-phenyl)-butyric acid methyl ester

Guidance literature:: With cyclohexene; palladium on activated charcoal; In ethanol; Heating;
DOI:10.1002/jps.2600770218

Reference yield:

: 1821-12-1
4-Phenylbutyric acid

: 113849-32-4
4-(2,4-Diamino-phenyl)-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 50 percent / HNO₃ / 6 h / Ambient temperature

2: HCl / Heating

3: 65 percent / cyclohexene / Pd/C / ethanol / Heating

With hydrogenchloride; nitric acid; cyclohexene; palladium on activated charcoal; In ethanol;
DOI:10.1002/jps.2600770218