(R)-2-((2-NITROPHENOXY)METHYL)OXIRANE

Base Information

Chemical Name:(R)-2-((2-NITROPHENOXY)METHYL)OXIRANE
CAS No.:345975-15-7
Molecular Formula:C9H9 N O4
Molecular Weight:195.175
Hs Code.:2910900090
Mol file:345975-15-7.mol

Synonyms:Oxirane,[(2-nitrophenoxy)methyl]-, (2R)- (9CI); (R)-Glycidyl o-nitrophenyl ether

Suppliers and Price of (R)-2-((2-NITROPHENOXY)METHYL)OXIRANE

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

American Custom Chemicals Corporation
(R)-2-((2-NITROPHENOXY)METHYL)OXIRANE 95.00%
5MG
$ 499.88

Total 3 raw suppliers

Chemical Property of (R)-2-((2-NITROPHENOXY)METHYL)OXIRANE

Chemical Property:

Boiling Point:341.4±12.0 °C(Predicted)
PSA：67.58000
Density:1.340±0.06 g/cm3(Predicted)
LogP:1.89560

Purity/Quality:

99% ^*data from raw suppliers

(R)-2-((2-NITROPHENOXY)METHYL)OXIRANE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (R)-2-((2-NITROPHENOXY)METHYL)OXIRANE

There total 4 articles about (R)-2-((2-NITROPHENOXY)METHYL)OXIRANE 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: 41.0%

: 21407-49-8
2-nitrophenyl glycidyl ether

: 345975-15-7
(R)-1,2-epoxy-3-(2-nitrophenoxy)propane

: 1227833-96-6
(R)-3-(2-nitrophenoxy)propane-1,2-diol

: 785817-21-2
(S)-3-(2-nitrophenoxy)propane-1,2-diol

Guidance literature:: With Bacillus megaterium ECU₁₀₀₁ epoxide hydrolase; In potassium phosphate buffer; dimethyl sulfoxide; at 30 ℃; for 1.5h; pH=7; optical yield given as %ee; enantioselective reaction; Resolution of racemate; Enzymatic reaction;
DOI:10.1002/adsc.201100031

Reference yield: 23.4%

: 21407-49-8
2-nitrophenyl glycidyl ether

: 345975-15-7
(R)-1,2-epoxy-3-(2-nitrophenoxy)propane

Guidance literature:: With sodium azide; recombinant alphaproteobacterium halohydrin dehalogenase; In ethanol; at 30 ℃; pH=7.5; enantioselective reaction; Resolution of racemate; Enzymatic reaction;
DOI:10.1007/s10562-019-02659-0

Reference yield:

: 88-75-5,78813-12-4
2-hydroxynitrobenzene

: 345975-15-7
(R)-1,2-epoxy-3-(2-nitrophenoxy)propane

Guidance literature:: 2-hydroxynitrobenzene; With sodium hydroxide; In N,N-dimethyl-formamide; for 0.5h;

(R)-glycidyl nosylate; In N,N-dimethyl-formamide; at 20 ℃; for 5h;
DOI:10.1038/s41429-019-0177-9