4-(bis(carboxymethyl)amino)benzoic Acid

Base Information

Chemical Name:4-(bis(carboxymethyl)amino)benzoic Acid
CAS No.:86364-45-6
Molecular Formula:C11H11NO6
Molecular Weight:253.211
Hs Code.:
ChEMBL ID:CHEMBL30503
DSSTox Substance ID:DTXSID40405671
Nikkaji Number:J2.752.484B
Wikidata:Q82210344

Synonyms:86364-45-6;4-(bis(carboxymethyl)amino)benzoic Acid;CHEMBL30503;SCHEMBL342127;DTXSID40405671;N-(4-carboxyphenyl)iminodiacetic acid;AKOS004117579

Suppliers and Price of 4-(bis(carboxymethyl)amino)benzoic Acid

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
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price

Total 1 raw suppliers

Chemical Property of 4-(bis(carboxymethyl)amino)benzoic Acid

Chemical Property:

XLogP3:0.8
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:6
Exact Mass:253.05863707
Heavy Atom Count:18
Complexity:318

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C(=O)O)N(CC(=O)O)CC(=O)O

Technology Process of 4-(bis(carboxymethyl)amino)benzoic Acid

There total 4 articles about 4-(bis(carboxymethyl)amino)benzoic Acid 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: 75.0%

: 86364-43-4
4-(Bis-ethoxycarbonylmethyl-amino)-benzoic acid ethyl ester

: 86364-45-6
N-(4-carboxyphenyl) iminodiacetic acid

Guidance literature:: With potassium hydroxide; In ethanol; water; for 3h; Heating;
DOI:10.1021/jm00364a011

Reference yield: 32.0%

: 150-13-0,159246-81-8,8014-65-1
4-amino-benzoic acid

: 79-11-8
chloroacetic acid

: 86364-45-6
N-(4-carboxyphenyl) iminodiacetic acid

Guidance literature:: With potassium hydroxide; In water; at 86 ℃; for 30h;
DOI:10.1002/ejic.200400218

Reference yield:

: 94-09-7
p-aminoethylbenzoate

: 86364-45-6
N-(4-carboxyphenyl) iminodiacetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / triethylamine, hexamethylphosphoramide / 18 h / 65 - 70 °C

2: 75 percent / KOH / ethanol; H₂O / 3 h / Heating

With N,N,N,N,N,N-hexamethylphosphoric triamide; potassium hydroxide; triethylamine; In ethanol; water;
DOI:10.1021/jm00364a011