4-Methoxybenzyl phenylcarbamate

Base Information

Chemical Name:4-Methoxybenzyl phenylcarbamate
CAS No.:68931-73-7
Molecular Formula:C15H15NO3
Molecular Weight:257.2845
Hs Code.:
NSC Number:131100
DSSTox Substance ID:DTXSID50299503
Wikidata:Q82041946

Synonyms:68931-73-7;4-methoxybenzyl phenylcarbamate;NSC131100;SCHEMBL11813314;DTXSID50299503;NSC-131100

Suppliers and Price of 4-Methoxybenzyl phenylcarbamate

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 5 raw suppliers

Chemical Property of 4-Methoxybenzyl phenylcarbamate

Chemical Property:

Vapor Pressure:1.55E-05mmHg at 25°C
Boiling Point:365.6°C at 760 mmHg
Flash Point:174.9°C
Density:1.204g/cm³
XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:257.10519334
Heavy Atom Count:19
Complexity:269

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)COC(=O)NC2=CC=CC=C2

Technology Process of 4-Methoxybenzyl phenylcarbamate

There total 2 articles about 4-Methoxybenzyl phenylcarbamate 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: 80.0%

: 495-18-1
Benzohydroxamic acid

: 105-13-5
4-Methoxybenzyl alcohol

: 68931-73-7
4-methoxybenzyl phenylcarbamate

Guidance literature:: Benzohydroxamic acid; With dmap; ethyl 2-(tert-butoxycarbonyloxyimino)-2-cyanoacetate; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 ℃; for 0.25h; Green chemistry;

4-Methoxybenzyl alcohol; In dichloromethane; at 60 ℃; for 6h; chemoselective reaction; Green chemistry;
DOI:10.1002/adsc.201600661