4-Amino-5-ethyl-isophthalic acid diethyl ester

Base Information

Chemical Name:4-Amino-5-ethyl-isophthalic acid diethyl ester
CAS No.:34921-57-8
Molecular Formula:C₁₄H₁₉NO₄
Molecular Weight:265.309
Hs Code.:
European Community (EC) Number:636-874-0

Synonyms:4-AMINO-5-ETHYL-ISOPHTHALIC ACID DIETHYL ESTER;AKOS024322837

Suppliers and Price of 4-Amino-5-ethyl-isophthalic acid diethyl ester

Supply Marketing:

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

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Chemical Property of 4-Amino-5-ethyl-isophthalic acid diethyl ester

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:7
Exact Mass:265.13140809
Heavy Atom Count:19
Complexity:319

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC1=C(C(=CC(=C1)C(=O)OCC)C(=O)OCC)N

Technology Process of 4-Amino-5-ethyl-isophthalic acid diethyl ester

There total 4 articles about 4-Amino-5-ethyl-isophthalic acid diethyl ester 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-Amino-5-ethoxycarbonimidoyl-3-ethyl-benzoic acid ethyl ester

: 34921-57-8
3-Aethyl-5-carbethoxyanthranilsaeureaethylester

Guidance literature:: With water;
DOI:10.1021/jo00983a011

Reference yield:

: 34921-60-3
5-bromo-7-ethylindoline-2,3-dione

: 34921-57-8
3-Aethyl-5-carbethoxyanthranilsaeureaethylester

Guidance literature:: Multi-step reaction with 5 steps

1: aq. NaOH, H₂O₂

2: HCl

3: N-methylpyrrolidone

4: HCl

5: H₂O

With 1-methyl-pyrrolidin-2-one; hydrogenchloride; sodium hydroxide; water; dihydrogen peroxide;
DOI:10.1021/jo00983a011