IPEROXO

Base Information

Chemical Name:IPEROXO
CAS No.:247079-84-1
Molecular Formula:C₁₀H₁₇N₂O₂*I
Molecular Weight:324.162
Hs Code.:

Synonyms:

Suppliers and Price of IPEROXO

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
Iperoxo ≥98% (HPLC)
5mg
$ 123.00

Sigma-Aldrich
Iperoxo ≥98% (HPLC)
25mg
$ 492.00

Cayman Chemical
Iperoxo (iodide)
10mg
$ 256.00

Cayman Chemical
Iperoxo (iodide)
5mg
$ 144.00

Cayman Chemical
Iperoxo (iodide)
1mg
$ 32.00

Total 5 raw suppliers

Chemical Property of IPEROXO

Chemical Property:

Storage Temp.:2-8°C
Solubility.:H2O: soluble5mg/mL, clear (warmed)

Purity/Quality:

98%,99%, ^*data from raw suppliers

Iperoxo ≥98% (HPLC) ^*data from reagent suppliers

Safty Information:

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

MSDS Files:

Useful:

Technology Process of IPEROXO

There total 3 articles about IPEROXO 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: 99.0%

: 247079-83-0
4-((4,5-dihydroisoxazol-3-yl)oxy)-N,N-dimethylbut-2-yn-1-amine

: 74-88-4
methyl iodide

: 247079-84-1
3-[4-(dimethylamino)-2-butynyl]oxy-Δ²-isoxazoline methiodide

Guidance literature:: In chloroform; at 20 ℃; for 24h;
DOI:10.1016/j.tetlet.2010.04.130

Reference yield:

: 247079-77-2
3-(4-hydroxy-2-butynyl)oxy-Δ²-isoxazoline

: 247079-84-1
3-[4-(dimethylamino)-2-butynyl]oxy-Δ²-isoxazoline methiodide

Guidance literature:: Multi-step reaction with 3 steps

1: 75 percent / triethylamine / CH₂Cl₂ / 5 h / 20 °C

2: 69 percent / methanol

3: diethyl ether / 20 °C

With triethylamine; In methanol; diethyl ether; dichloromethane; 1: Esterification / 2: Alkylation / 3: Methylation;
DOI:10.1016/S0968-0896(99)00107-8

Reference yield:

: 247079-78-3
3-(4-hydroxy-2-butynyl)oxy-Δ²-isoxazoline mesylate

: 247079-84-1
3-[4-(dimethylamino)-2-butynyl]oxy-Δ²-isoxazoline methiodide

Guidance literature:: Multi-step reaction with 2 steps

1: 69 percent / methanol

2: diethyl ether / 20 °C

In methanol; diethyl ether; 1: Alkylation / 2: Methylation;
DOI:10.1016/S0968-0896(99)00107-8