2-METHOXYPHENYLZINC IODIDE 0.5M

Base Information

Chemical Name:2-METHOXYPHENYLZINC IODIDE 0.5M
CAS No.:282727-20-2
Molecular Formula:C7H7 I O Zn
Molecular Weight:299.426
Hs Code.:
Mol file:282727-20-2.mol

Synonyms:(2-Methoxyphenyl)zinciodide

Suppliers and Price of 2-METHOXYPHENYLZINC IODIDE 0.5M

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
2-Methoxyphenylzinc iodide solution 0.5M in THF
50ml
$ 136.00

Rieke Metals
2-Methoxyphenylzinciodide
100mL
$ 448.00

Rieke Metals
2-Methoxyphenylzinciodide
50mL
$ 263.00

American Custom Chemicals Corporation
2-METHOXYPHENYLZINC IODIDE 95.00%
1L
$ 8085.00

American Custom Chemicals Corporation
2-METHOXYPHENYLZINC IODIDE 95.00%
500ML
$ 5428.50

American Custom Chemicals Corporation
2-METHOXYPHENYLZINC IODIDE 95.00%
100ML
$ 2783.55

Alfa Aesar
2-Methoxyphenylzinc iodide, 0.5M in THF, packaged under Argon in resealable ChemSeal? bottles
50ml
$ 132.00

Total 7 raw suppliers

Chemical Property of 2-METHOXYPHENYLZINC IODIDE 0.5M

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：9.23000
Density:g/cm³
LogP:2.37860
Storage Temp.:2-8°C
Sensitive.:Air & Light Sensitive

Purity/Quality:

99% ^*data from raw suppliers

2-Methoxyphenylzinc iodide solution 0.5M in THF ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:F,Xn
Statements: 19-22-36/38-40-36/37-14-11
Safety Statements: 16-26-33-36-36/37

MSDS Files:: SDS file from LookChem

Useful:

Uses 2-Methoxyphenylzinc iodide can be used:As a substrate in the synthesis of aryl ketones by reacting with aroyl chlorides.As a starting material in the synthesis of sulfones by reacting with DABSO reagent and alkyl halides.

Technology Process of 2-METHOXYPHENYLZINC IODIDE 0.5M

There total 1 articles about 2-METHOXYPHENYLZINC IODIDE 0.5M 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:

: 529-28-2
4-iodoanisol

: 7440-66-6
zinc

: 282727-20-2
(2-methoxyphenyl)zinc(II) iodide

Guidance literature:: In further solvent(s); Sonication; (N2); solvent = 1,1,3,3-tetramethylurea; 2 equivs. of Zn powder used; 50 °C; ultrasound applied for 20 h; 61% conversion; not isolated; conversion detd. by quenching with I2;
DOI:10.1246/cl.1993.469

Reference yield: 93.0%

: 879-18-5
naphthalene-1-carbonic acid chloride

: 282727-20-2
(2-methoxyphenyl)zinc(II) iodide

: (2-methoxyphenyl)-1-naphthylmethanone

Guidance literature:: With bis(acetylacetonate)nickel(II); In tetrahydrofuran; at 20 ℃; for 0.5h;
DOI:10.5012/bkcs.2012.33.9.3083

Reference yield: 90.0%

: 591-50-4
iodobenzene

: 282727-20-2
(2-methoxyphenyl)zinc(II) iodide

: 86-26-0,292625-97-9
2-methoxy-1,1'-biphenyl

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,2-dimethoxyethane; at 60 ℃; for 24h; Inert atmosphere;
DOI:10.1002/ejoc.201801543