N-(2-Naphthyl)-3-oxobutanamide

Base Information

Chemical Name:N-(2-Naphthyl)-3-oxobutanamide
CAS No.:42414-19-7
Molecular Formula:C14H13NO2
Molecular Weight:227.263
Hs Code.:
NSC Number:165883
DSSTox Substance ID:DTXSID90304483
Nikkaji Number:J1.426.727A
Wikidata:Q82050418
ChEMBL ID:CHEMBL1330594

Synonyms:42414-19-7;N-(2-Naphthyl)-3-oxobutanamide;N-2-naphthyl-3-oxobutanamide;N-naphthalen-2-yl-3-oxobutanamide;NSC165883;N-(Naphthalen-2-yl)-3-oxobutanamide;MLS000756355;CHEMBRDG-BB 6084045;NSC-165883;N-(2-Naphthyl)acetoacetamide;CBMicro_010011;NCIStruc1_000884;NCIStruc2_000820;SCHEMBL9291930;CHEMBL1330594;DTXSID90304483;SJZXYYGWOBQVKI-UHFFFAOYSA-N;HMS2885O08;SMSF0013685;N-(2-Naphthyl)-3-oxobutanamide #;CCG-38077;MFCD01001280;NCGC00014465;NCI165883;AKOS000165525;CB12891;NCGC00014465-02;NCGC00097570-01;BS-37767;NCI60_001280;SMR000528695;BIM-0009946.P001;SR-01000227079;SR-01000227079-1

Suppliers and Price of N-(2-Naphthyl)-3-oxobutanamide

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 6 raw suppliers

Chemical Property of N-(2-Naphthyl)-3-oxobutanamide

Chemical Property:

Vapor Pressure:4.62E-09mmHg at 25°C
Boiling Point:471.5°C at 760 mmHg
Flash Point:198.8°C
Density:1.216g/cm³
XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:227.094628657
Heavy Atom Count:17
Complexity:301

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)CC(=O)NC1=CC2=CC=CC=C2C=C1

Technology Process of N-(2-Naphthyl)-3-oxobutanamide

There total 7 articles about N-(2-Naphthyl)-3-oxobutanamide 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: 55.0%

: 454713-47-4
tert-butyl (1-bromonaphthalen-2-yl)carbamate

: 108-24-7
acetic anhydride

: 42414-19-7
N-(naphthalen-2-yl)-3-oxobutanamide

: tert-butyl (1-acetylnaphthalen-2-yl)carbamate

: 454713-45-2
naphthalen-2-yl-carbamic acid tert-butyl ester

Guidance literature:: tert-butyl (1-bromonaphthalen-2-yl)carbamate; With n-butyllithium; In diethyl ether; at -20 ℃; for 2h; Schlenk technique; Inert atmosphere;

acetic anhydride; In diethyl ether; at -78 ℃; for 2h; Schlenk technique; Inert atmosphere;
DOI:10.24820/ark.5550190.p010.739