4-(Dodecanoylamino)benzoic acid

Base Information

Chemical Name:4-(Dodecanoylamino)benzoic acid
CAS No.:58725-40-9
Molecular Formula:C19H29NO3
Molecular Weight:319.444
Hs Code.:
European Community (EC) Number:685-945-2
DSSTox Substance ID:DTXSID30405645
Nikkaji Number:J2.441.098F
Wikidata:Q82210300

Synonyms:58725-40-9;4-(dodecanoylamino)benzoic acid;4-DODECANAMIDOBENZOIC ACID;SCHEMBL76386;DTXSID30405645;YMAAMSKAPGRCCN-UHFFFAOYSA-N;p-(N-Dodecanoylamino)-Benzoic Acid;N-(n-dodecanoyl)-p-aminobenzoic acid;AKOS001584761

Suppliers and Price of 4-(Dodecanoylamino)benzoic acid

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 4-(Dodecanoylamino)benzoic acid

Chemical Property:

PSA：66.40000
LogP:5.31720
XLogP3:5.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:12
Exact Mass:319.21474379
Heavy Atom Count:23
Complexity:336

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCC(=O)NC1=CC=C(C=C1)C(=O)O

Technology Process of 4-(Dodecanoylamino)benzoic acid

There total 5 articles about 4-(Dodecanoylamino)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:

: 112-16-3
n-dodecanoyl chloride

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

: 58725-40-9
N-dodecanoyl-p-amino benzoic acid

Guidance literature:: With pyridine;

Reference yield:

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

: 58725-40-9
N-dodecanoyl-p-amino benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: HCl / methanol / 2 h / 0 °C

1.2: methanol / 4 h / Heating

2.1: Et₃N / CH₂Cl₂ / 3 h / 0 °C

3.1: 3.67 g / KOH / methanol / 10 h / 20 °C

With hydrogenchloride; potassium hydroxide; triethylamine; In methanol; dichloromethane;
DOI:10.1021/ja0676197

Reference yield:

: 619-45-4
4-methoxycarbonyl aniline

: 58725-40-9
N-dodecanoyl-p-amino benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 3 h / 0 °C

2: 3.67 g / KOH / methanol / 10 h / 20 °C

With potassium hydroxide; triethylamine; In methanol; dichloromethane;
DOI:10.1021/ja0676197