Hydroxyphenyl propamidobenzoic acid

Base Information

Chemical Name:Hydroxyphenyl propamidobenzoic acid
CAS No.:697235-49-7
Molecular Formula:C₁₆H₁₅NO₄
Molecular Weight:285.299
Hs Code.:
European Community (EC) Number:470-130-4,690-968-6
UNII:25KRT26H77
DSSTox Substance ID:DTXSID80220022
Nikkaji Number:J2.530.302D
Wikidata:Q27253970
RXCUI:1427188
Mol file:697235-49-7.mol

Synonyms:2-((3-(4-hydroxyphenyl)-1-oxopropyl)amino)benzoic acid;DHAvD cpd;dihydroavenanthramide D

Suppliers and Price of Hydroxyphenyl propamidobenzoic 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 61 raw suppliers

Chemical Property of Hydroxyphenyl propamidobenzoic acid

Chemical Property:

Vapor Pressure:0Pa at 20℃
Boiling Point:590.0±40.0 °C(Predicted)
PKA:3.47±0.10(Predicted)
PSA：90.12000
Density:1.354±0.06 g/cm3(Predicted)
LogP:3.31120
Water Solubility.:86.5mg/L at 20℃
XLogP3:3.4
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:285.10010796
Heavy Atom Count:21
Complexity:363

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C(=O)O)NC(=O)CCC2=CC=C(C=C2)O
Uses 2-(3-(4-hydroxyphenyl)propanamido)benzoic acid can be used as a raw material for cosmetics, It works as a skin soothing agent thanks to its triple anti-irritant benefits: reduces redness, inflammation and itch PLUS has anti-oxidant efficacy.

Technology Process of Hydroxyphenyl propamidobenzoic acid

There total 8 articles about Hydroxyphenyl propamidobenzoic 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: 89.0%

: C₁₈H₁₇NO₅

: 697235-49-7
2-(3-(4-hydroxyphenyl)propionamido)benzoic acid

Guidance literature:: With sodium hydroxide; for 0.5h; pH=4.5;

Reference yield:

: 501-97-3
4-hydroxyphenylpropionic acid

: 118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4
anthranilic acid

: 697235-49-7
2-(3-(4-hydroxyphenyl)propionamido)benzoic acid

Guidance literature:: With pDRf₁-(4-coumaroyl:CoA ligase 5 from Arabidopsis thaliana)-(hydroxycinnamoyl/benzoyl-CoA:anthranilate N-hydroxycinnamoyl/benzoyltransferase 1 from Dianthus caryophyllus) recombinant yeast; In dimethyl sulfoxide; at 30 ℃; for 24h;
DOI:10.1371/journal.pone.0138972

Reference yield:

: 2-[(p-ethanoyloxy)phenylpropanoylamino]benzoic acid methyl ester

: 697235-49-7
2-(3-(4-hydroxyphenyl)propionamido)benzoic acid

Guidance literature:: 2-[(p-ethanoyloxy)phenylpropanoylamino]benzoic acid methyl ester; With ethanol; sodium hydroxide; at 60 - 70 ℃; for 3h;

With hydrogenchloride; ethanol; In water; for 1h; pH=1 - 3;