Ethyl (7-hydroxy-1-naphthyl)-carbamate

Base Information

Chemical Name:Ethyl (7-hydroxy-1-naphthyl)-carbamate
CAS No.:68214-72-2
Molecular Formula:C13H13NO3
Molecular Weight:231.251
Hs Code.:
European Community (EC) Number:269-311-9
DSSTox Substance ID:DTXSID9071264
Nikkaji Number:J60.030J
Wikidata:Q81998850
Mol file:68214-72-2.mol

Synonyms:68214-72-2;Ethyl (7-hydroxy-1-naphthyl)-carbamate;Ethyl (7-hydroxy-1-napthalenyl)carbamate;ethyl (7-hydroxynaphthalen-1-yl)carbamate;EINECS 269-311-9;Ethyl N-(7-hydroxynaphth-1-yl) carbamate;Carbamic acid, (7-hydroxy-1-naphthalenyl)-, ethyl ester;Carbamic acid, N-(7-hydroxy-1-naphthalenyl)-, ethyl ester;ethyl N-(7-hydroxynaphthalen-1-yl)carbamate;SCHEMBL4808201;DTXSID9071264;AKOS024405741;ETHYL 7-HYDROXY-1-NAPHTHYLCARBAMATE;7-Hydroxy-1-naphthalenecarbamic acid ethyl ester

Suppliers and Price of Ethyl (7-hydroxy-1-naphthyl)-carbamate

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 4 raw suppliers

Chemical Property of Ethyl (7-hydroxy-1-naphthyl)-carbamate

Chemical Property:

Vapor Pressure:4.11E-06mmHg at 25°C
Boiling Point:373.6°Cat760mmHg
Flash Point:179.8°C
PSA：62.05000
Density:1.299g/cm³
LogP:3.12740
XLogP3:2.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:231.08954328
Heavy Atom Count:17
Complexity:269

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)NC1=CC=CC2=C1C=C(C=C2)O

Technology Process of Ethyl (7-hydroxy-1-naphthyl)-carbamate

There total 1 articles about Ethyl (7-hydroxy-1-naphthyl)-carbamate 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:

: 118-46-7
8-amino-2-naphthol

: 541-41-3
chloroformic acid ethyl ester

: 68214-72-2
(7-hydroxy-[1]naphthyl)-carbamic acid ethyl ester

Guidance literature:

Reference yield:

: 68214-72-2
(7-hydroxy-[1]naphthyl)-carbamic acid ethyl ester

: (7,8-dioxo-5-phenyl-7,8-dihydro-naphthalen-1-yl)-carbamic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: (PhSeO)2O / tetrahydrofuran / 50 °C

2: Pd(OAc); AcOH / Heating

With palladium diacetate; (PhSeO)2O; acetic acid; In tetrahydrofuran;
DOI:10.1016/S0960-894X(02)00331-1