4-[(3,4,5-trimethoxybenzoyl)amino]butanoic Acid

Base Information

Chemical Name:4-[(3,4,5-trimethoxybenzoyl)amino]butanoic Acid
CAS No.:32407-13-9
Molecular Formula:C14H19NO6
Molecular Weight:297.308
Hs Code.:
DSSTox Substance ID:DTXSID20364838
Wikidata:Q82149014
Mol file:32407-13-9.mol

Synonyms:4-[(3,4,5-trimethoxybenzoyl)amino]butanoic Acid;32407-13-9;Butanoic acid, 4-[(3,4,5-trimethoxybenzoyl)amino]-;4-[(3,4,5-TRIMETHOXYPHENYL)FORMAMIDO]BUTANOIC ACID;4-{[(3,4,5-trimethoxyphenyl)carbonyl]amino}butanoic acid;SCHEMBL2677556;DTXSID20364838;BBL036198;STL261792;AKOS000132566;VS-13364;4-(3,4,5-Trimethoxybenzamido)butanoic acid;CS-0333017;SR-01000106249;SR-01000106249-1

Suppliers and Price of 4-[(3,4,5-trimethoxybenzoyl)amino]butanoic 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
Packaging
price

Total 2 raw suppliers

Chemical Property of 4-[(3,4,5-trimethoxybenzoyl)amino]butanoic Acid

Chemical Property:

PSA：97.58000
LogP:1.88180
XLogP3:1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:8
Exact Mass:297.12123733
Heavy Atom Count:21
Complexity:334

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC(=CC(=C1OC)OC)C(=O)NCCCC(=O)O

Technology Process of 4-[(3,4,5-trimethoxybenzoyl)amino]butanoic Acid

There total 3 articles about 4-[(3,4,5-trimethoxybenzoyl)amino]butanoic 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: 99.0%

: 58345-09-8
4-(3,4,5-trimethoxy-benzoylamino)-butyric acid ethyl ester

: 32407-13-9
N-(3,4,5-trimethoxybenzoyl)-γ-aminobutyric acid

Guidance literature:: With lithium hydroxide; In acetonitrile; at 20 ℃; for 18h;
DOI:10.1021/jm060536g

Reference yield:

: 4521-61-3
3,4,5-Trimethoxybenzoyl chloride

: 32407-13-9
N-(3,4,5-trimethoxybenzoyl)-γ-aminobutyric acid

Guidance literature:: Multi-step reaction with 2 steps

1: 58 percent / Et₃N / CH₂Cl₂ / 24 h / 20 °C

2: 99 percent / aq. LiOH / acetonitrile / 18 h / 20 °C

With lithium hydroxide; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1021/jm060536g