2-Propenoic acid, 2-(acetylamino)-3-(1-naphthalenyl)-, (Z)-

Base Information

Chemical Name:2-Propenoic acid, 2-(acetylamino)-3-(1-naphthalenyl)-, (Z)-
CAS No.:88681-65-6
Molecular Formula:C15H13NO3
Molecular Weight:
Hs Code.:
DSSTox Substance ID:DTXSID20406363

Synonyms:2-Propenoic acid, 2-(acetylamino)-3-(1-naphthalenyl)-, (Z)-;88681-65-6;DTXSID20406363

Suppliers and Price of 2-Propenoic acid, 2-(acetylamino)-3-(1-naphthalenyl)-, (Z)-

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 1 raw suppliers

Chemical Property of 2-Propenoic acid, 2-(acetylamino)-3-(1-naphthalenyl)-, (Z)-

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:255.08954328
Heavy Atom Count:19
Complexity:389

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC(=CC1=CC=CC2=CC=CC=C21)C(=O)O

Technology Process of 2-Propenoic acid, 2-(acetylamino)-3-(1-naphthalenyl)-, (Z)-

There total 3 articles about 2-Propenoic acid, 2-(acetylamino)-3-(1-naphthalenyl)-, (Z)- 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: 92.0%

: 128858-50-4
(Z)-2-methyl-4-(naphthalen-1-ylmethylene)oxazol-5(4H)-one

: 88681-65-6
(Z)-2-Acetylamino-3-naphthalen-1-yl-acrylic acid

Guidance literature:: With sodium hydroxide; In methanol; at 20 ℃; for 0.5h;
DOI:10.1080/00397910701265895

Reference yield: 60.0%

: 5429-56-1
N-Acetamidoacrylic acid

: 90-11-9
1-Bromonaphthalene

: 88681-65-6
(Z)-2-Acetylamino-3-naphthalen-1-yl-acrylic acid

Guidance literature:: With triethylamine; palladium diacetate; triphenylphosphine; at 110 ℃; for 22h;
DOI:10.1016/S0040-4039(00)85967-5

Reference yield:

: 66-77-3
1-naphthaldehyde

: 88681-65-6
(Z)-2-Acetylamino-3-naphthalen-1-yl-acrylic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium acetate; acetic anhydride / 0.5 h / 20 °C

1.2: 80 percent / 5 h / 60 °C

2.1: 92 percent / aq. sodium hydroxide / methanol / 0.5 h / 20 °C

With sodium hydroxide; sodium acetate; acetic anhydride; In methanol;
DOI:10.1080/00397910701265895