6-[(4-Methoxybenzoyl)amino]hexanoic acid

Base Information

Chemical Name:6-[(4-Methoxybenzoyl)amino]hexanoic acid
CAS No.:22834-47-5
Molecular Formula:C₁₄H₁₉NO₄
Molecular Weight:265.309
Hs Code.:
DSSTox Substance ID:DTXSID101277413
Nikkaji Number:J1.216.518H
ChEMBL ID:CHEMBL346433
Mol file:22834-47-5.mol

Synonyms:6-[(4-methoxybenzoyl)amino]hexanoic acid;22834-47-5;Hexanoic acid, 6-[(4-methoxybenzoyl)amino]-;6-(4-Methoxy-benzoylamino)-hexanoic acid;CBDivE_011081;CHEMBL346433;SCHEMBL1233294;DTXSID101277413;6-(4-Methoxybenzamido)hexanoic acid;STK091269;AKOS000136839;CS-0328284;6-{[(4-methoxyphenyl)carbonyl]amino}hexanoic acid

Suppliers and Price of 6-[(4-Methoxybenzoyl)amino]hexanoic 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

Matrix Scientific
6-[(4-Methoxybenzoyl)amino]hexanoic acid
10g
$ 1170.00

Matrix Scientific
6-[(4-Methoxybenzoyl)amino]hexanoic acid
5g
$ 810.00

Matrix Scientific
6-[(4-Methoxybenzoyl)amino]hexanoic acid
1g
$ 316.00

Aronis compounds
6-[(4-methoxybenzoyl)amino]hexanoicacid
5mg
$ 15.00

American Custom Chemicals Corporation
6-(4-METHOXY-BENZOYLAMINO)-HEXANOIC ACID 95.00%
5MG
$ 505.85

Total 2 raw suppliers

Chemical Property of 6-[(4-Methoxybenzoyl)amino]hexanoic acid

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:8
Exact Mass:265.13140809
Heavy Atom Count:19
Complexity:285

Purity/Quality:

99% ^*data from raw suppliers

6-[(4-Methoxybenzoyl)amino]hexanoic acid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC=C(C=C1)C(=O)NCCCCCC(=O)O

Technology Process of 6-[(4-Methoxybenzoyl)amino]hexanoic acid

There total 5 articles about 6-[(4-Methoxybenzoyl)amino]hexanoic 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: 98.0%

: 251456-91-4
methyl 6-(4-methoxybenzoyl)aminocaproate

: 22834-47-5
N-(4-methoxybenzoyl)-6-aminohexanoic acid

Guidance literature:

Reference yield: 95.0%

: 100-07-2
4-methoxy-benzoyl chloride

: 60-32-2,93208-38-9
6-aminohexanoic acid

: 22834-47-5
N-(4-methoxybenzoyl)-6-aminohexanoic acid

Guidance literature:: With sodium hydroxide; In tetrahydrofuran; for 2h;

Reference yield:

: 1926-80-3
methyl 6-aminocaproate hydrochloride

: 22834-47-5
N-(4-methoxybenzoyl)-6-aminohexanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / TEA / CH₂Cl₂ / 3.5 h / 5 - 20 °C

2: 72 percent / 1M aq. LiOH / tetrahydrofuran / 4 h / 20 °C

With lithium hydroxide; TEA; In tetrahydrofuran; dichloromethane; 1: Acylation / 2: Hydrolysis;
DOI:10.1021/jm991091h