Carbamic acid, (3-oxiranylpropyl)-, 1,1-dimethylethyl ester (9CI)

Base Information

Chemical Name:Carbamic acid, (3-oxiranylpropyl)-, 1,1-dimethylethyl ester (9CI)
CAS No.:220243-54-9
Molecular Formula:C10H19 N O3
Molecular Weight:201.266
Hs Code.:
Mol file:220243-54-9.mol

Synonyms:(3-oxiranylpropyl)carbamic acid tert-butyl ester;;(3-Oxiranyl-propyl)-carbamic acid tert-butyl ester;;40462 TERT-BUTYL 3-(OXIRAN-2-YL)PROPYLCARBAMATE;;

Suppliers and Price of Carbamic acid, (3-oxiranylpropyl)-, 1,1-dimethylethyl ester (9CI)

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
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Total 7 raw suppliers

Chemical Property of Carbamic acid, (3-oxiranylpropyl)-, 1,1-dimethylethyl ester (9CI)

Chemical Property:

Appearance/Colour:chemical research
Boiling Point:296.066°C at 760 mmHg (Cal.) ref.
Flash Point:132.856°C (Cal.) ref.
PSA：50.86000
Density:1.041g/cm3 (Cal.) ref.
LogP:2.08100

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Carbamic acid, (3-oxiranylpropyl)-, 1,1-dimethylethyl ester (9CI)

There total 1 articles about Carbamic acid, (3-oxiranylpropyl)-, 1,1-dimethylethyl ester (9CI) 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:

: 6404-29-1
6-(tert-butoxycarbonylamino)hexanoic acid

: 220243-54-9
((rac)-3-oxiranyl-propyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 32 percent / Cu(OAc)2*H₂O; Pb(OAc)4 / benzene / 6.5 h / Heating

2: 96 percent / m-CPBA / CH₂Cl₂ / 16 h / 20 °C

With lead(IV) acetate; copper diacetate; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; benzene; 1: Decarboxylation / 2: Epoxidation;
DOI:10.1016/S0040-4020(98)01023-0