Tert-butyl benzoyloxycarbamate

Base Information Edit

Chemical Name:Tert-butyl benzoyloxycarbamate
CAS No.:105340-85-0
Molecular Formula:C12H15NO4
Molecular Weight:237.255
Hs Code.:
European Community (EC) Number:806-063-8
Nikkaji Number:J989.989H
Mol file:105340-85-0.mol

Synonyms:tert-butyl benzoyloxycarbamate;105340-85-0;[(tert-Butoxy)carbonyl]amino benzoate;[(2-methylpropan-2-yl)oxycarbonylamino] Benzoate;SCHEMBL1948795;KMXMOOQVJSFNNK-UHFFFAOYSA-N;AS-60074;(Benzoyloxy)carbamic acid tert-butyl ester;tert-Butyl benzoyloxycarbamate, AldrichCPR;benzoic acid (tert-butoxycarbonylamino) ester;D93365

Suppliers and Price of Tert-butyl benzoyloxycarbamate

Supply Marketing:Edit

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

aablocks
tert-Butylbenzoyloxycarbamate 95%
1g
$ 400.00

Total 1 raw suppliers

Chemical Property of Tert-butyl benzoyloxycarbamate Edit

Chemical Property:

PSA：64.63000
LogP:2.67400
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:237.10010796
Heavy Atom Count:17
Complexity:277

Purity/Quality:: tert-Butylbenzoyloxycarbamate 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 26

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NOC(=O)C1=CC=CC=C1

Technology Process of Tert-butyl benzoyloxycarbamate

There total 11 articles about Tert-butyl benzoyloxycarbamate 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: 99.0%