benzyl N-(2-oxooxolan-3-yl)carbamate

Base Information

Chemical Name:benzyl N-(2-oxooxolan-3-yl)carbamate
CAS No.:31332-88-4
Molecular Formula:C12H13 N O4
Molecular Weight:235.24
Hs Code.:
NSC Number:177385,293565
Nikkaji Number:J1.621.381K
ChEMBL ID:CHEMBL1880543
Mol file:31332-88-4.mol

Synonyms:benzyl N-(2-oxooxolan-3-yl)carbamate;31332-88-4;Cbz-DL-homoserine lactone;MLS003106886;benzyl N-(2-oxotetrahydrofuran-3-yl)carbamate;N-Cbz-D-homoserine lactone;MFCD00674555;MFCD11519127;NSC293565;Cbz-D-Homoser lactone;SCHEMBL7511180;CHEMBL1880543;FKWDZIFOVOUDAG-UHFFFAOYSA-N;BCP20063;benzylN-(2-oxooxolan-3-yl)carbamate;NSC177385;AKOS024375449;NSC-177385;NSC-293565;SMR001821771;SY030472;SY113808;Benzyl (2-oxotetrahydrofuran-3-yl)carbamate;Benzyl 2-oxotetrahydro-3-furanylcarbamate #;CS-0377050;FT-0603906;FT-0603907;EN300-217805;F78756;A903577;Z33609327;Carbamate, N-(2-oxotetrahydro-3-furanyl)-, benzyl ester

Suppliers and Price of benzyl N-(2-oxooxolan-3-yl)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 7 raw suppliers

Chemical Property of benzyl N-(2-oxooxolan-3-yl)carbamate

Chemical Property:

Vapor Pressure:7.29E-09mmHg at 25°C
Boiling Point:466.1°C at 760 mmHg
Flash Point:235.7°C
Density:1.27g/cm³
XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:235.08445790
Heavy Atom Count:17
Complexity:286

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COC(=O)C1NC(=O)OCC2=CC=CC=C2

Technology Process of benzyl N-(2-oxooxolan-3-yl)carbamate

There total 13 articles about benzyl N-(2-oxooxolan-3-yl)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: 97.0%

: 6305-38-0
α-amino-γ-butyrolactone hydrobromide

: 501-53-1,94274-21-2
benzyl chloroformate

: 31332-88-4
(S)-3-(N-benzyloxycarbonylamino)tetrahydrofuran-2-one

Guidance literature:: With triethylamine; In chloroform; at 20 ℃;
DOI:10.1002/jlcr.544

Reference yield: 87.0%

: (x)BrH*C₄H₇NO₂

: 501-53-1,94274-21-2
benzyl chloroformate

: 31332-88-4
(S)-3-(N-benzyloxycarbonylamino)tetrahydrofuran-2-one

Guidance literature:: (x)BrH*C₄H₇NO₂; benzyl chloroformate; With triethylamine; In tetrahydrofuran; at 0 - 20 ℃; for 17h; Inert atmosphere;

With hydrogenchloride; In water; pH=3;