2-(4-Nitrophenyl)morpholine

Base Information

Chemical Name:2-(4-Nitrophenyl)morpholine
CAS No.:61192-65-2
Molecular Formula:C10H12N2O3
Molecular Weight:208.217
Hs Code.:
ChEMBL ID:CHEMBL3303697
DSSTox Substance ID:DTXSID30501010

Synonyms:2-(4-NITROPHENYL)MORPHOLINE;61192-65-2;SCHEMBL5118709;CHEMBL3303697;DTXSID30501010;SGUCKOYGKLBSOC-UHFFFAOYSA-N;MFCD14529174;AKOS022271922;NS-02290;CS-0146438

Suppliers and Price of 2-(4-Nitrophenyl)morpholine

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

TRC
2-(4-Nitrophenyl)morpholine
25mg
$ 175.00

TRC
2-(4-Nitrophenyl)morpholine
5mg
$ 60.00

Crysdot
2-(4-Nitrophenyl)morpholine 95+%
1g
$ 794.00

Chemenu
2-(4-Nitrophenyl)morpholine 95%
1g
$ 750.00

Chemcia Scientific
2-(4-Nitro-phenyl)-morpholine 95%
1 G
$ 440.00

Alichem
2-(4-Nitrophenyl)morpholine
1g
$ 878.80

Alichem
2-(4-Nitrophenyl)morpholine
250mg
$ 361.66

Total 6 raw suppliers

Chemical Property of 2-(4-Nitrophenyl)morpholine

Chemical Property:

PSA：67.08000
LogP:2.10770
XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:208.08479225
Heavy Atom Count:15
Complexity:221

Purity/Quality:

99% ^*data from raw suppliers

2-(4-Nitrophenyl)morpholine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COC(CN1)C2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of 2-(4-Nitrophenyl)morpholine

There total 5 articles about 2-(4-Nitrophenyl)morpholine 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: 83.0%

: 1393901-42-2
2-(4-nitrophenyl)-4-tosylmorpholine

: 61192-65-2
2-(4-nitrophenyl)morpholine

Guidance literature:: With hydrogen bromide; acetic acid; phenol; at 75 ℃; for 20h; Sealed tube;

Reference yield:

: 6388-74-5,38201-14-8,71884-55-4
p-Nitrophenyloxirane

: 61192-65-2
2-(4-nitrophenyl)morpholine

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate; N-benzyl-N,N,N-triethylammonium chloride / 1,4-dioxane / 4 h / 90 °C

2.1: sodium hydride / dichloromethane / 0.17 h / 0 °C / Inert atmosphere

2.2: 17 h / 20 °C / Cooling with ice

3.1: hydrogen bromide; acetic acid; phenol / 12 h / 75 °C / sealed tube; microwave irradiation

With N-benzyl-N,N,N-triethylammonium chloride; hydrogen bromide; sodium hydride; potassium carbonate; acetic acid; phenol; In 1,4-dioxane; dichloromethane;

Reference yield:

: 99-81-0
4-Nitrophenacyl bromide

: 61192-65-2
2-(4-nitrophenyl)morpholine

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium tetrahydroborate; methanol / 3 h / 20 °C / Cooling with ice

1.2: 16 h / 20 °C

2.1: potassium carbonate; N-benzyl-N,N,N-triethylammonium chloride / 1,4-dioxane / 4 h / 90 °C

3.1: sodium hydride / dichloromethane / 0.17 h / 0 °C / Inert atmosphere

3.2: 17 h / 20 °C / Cooling with ice

4.1: hydrogen bromide; acetic acid; phenol / 12 h / 75 °C / sealed tube; microwave irradiation

With methanol; sodium tetrahydroborate; N-benzyl-N,N,N-triethylammonium chloride; hydrogen bromide; sodium hydride; potassium carbonate; acetic acid; phenol; In 1,4-dioxane; dichloromethane;