N-IodoMorpholine hydriodide

Base Information

Chemical Name:N-IodoMorpholine hydriodide
CAS No.:120972-13-6
Molecular Formula:C4H9I2NO
Molecular Weight:340.931
Hs Code.:2934999090
Mol file:120972-13-6.mol

Synonyms:N-IodoMorpholine hydriodide;4-iodoMorpholine hydroiodide;Morpholine-iodide adduct;N-Iodomorpholinium iodide

Suppliers and Price of N-IodoMorpholine hydriodide

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

Sigma-Aldrich
N-Iodomorpholine hydriodide 97%
5g
$ 118.00

Sigma-Aldrich
N-Iodomorpholine hydriodide 97%
1g
$ 36.70

Total 1 raw suppliers

Chemical Property of N-IodoMorpholine hydriodide

Chemical Property:

Melting Point:92-96°C
PSA：12.47000
LogP:1.60470
Storage Temp.:2-8°C

Purity/Quality:: N-Iodomorpholine hydriodide 97% ^*data from reagent suppliers

Safty Information:

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

MSDS Files:

Useful:

Uses N-Iodomorpholine hydriodide is an iodinating reagent that can be used in:The iodination of (4-ethynylphenyl)diphenylphosphine oxide to yield (4-(iodoethynyl)phenyl)diphenylphosphine oxide, which is further used to prepare phosphine oxide-iodotriazole hybrid molecules.The synthesis of silver bis(pyrazolyl)-methane complex based supramolecular architectures.The synthesis of iodo-1,4-naphthoquinones, which are used to prepare biologically significant 3-aryl-1,4-naphthoquinones.

Technology Process of N-IodoMorpholine hydriodide

There total 1 articles about N-IodoMorpholine hydriodide 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: 89.0%

: 110-91-8,99108-56-2
morpholine

: 120972-13-6
N-iodomorpholine-hydrogen iodide

Guidance literature:: With iodine; In methanol;
DOI:10.1002/anie.200903558

Reference yield: 56.0%

: 1019202-25-5
ethynyl(phenyl)carbamic acid tert-butyl ester

: 120972-13-6
N-iodomorpholine-hydrogen iodide

: tert-butyl (2,2-diiodo-1-morpholinovinyl)(phenyl)carbamate

: tert-butyl phenyl(1,2,2-triiodovinyl)carbamate

Guidance literature:: With tert.-butylhydroperoxide; In water; toluene; at 20 ℃; for 12h; regioselective reaction; Schlenk technique;
DOI:10.1039/c6cc00370b