3-Iodo-5-methylaniline

Base Information

Chemical Name:3-Iodo-5-methylaniline
CAS No.:74586-54-2
Molecular Formula:C₇H₈IN
Molecular Weight:0
Hs Code.:
European Community (EC) Number:863-345-3
DSSTox Substance ID:DTXSID60599420

Synonyms:3-Iodo-5-methylaniline;74586-54-2;SCHEMBL8773072;DTXSID60599420;LOUHGQOWBDORSI-UHFFFAOYSA-N;AKOS033752144;DA-20391;EN300-209574;G71381;Z1269159888

Suppliers and Price of 3-Iodo-5-methylaniline

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

Total 6 raw suppliers

Chemical Property of 3-Iodo-5-methylaniline

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:232.97015
Heavy Atom Count:9
Complexity:94.9

Purity/Quality:: 98%Min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=CC(=C1)I)N

Technology Process of 3-Iodo-5-methylaniline

There total 6 articles about 3-Iodo-5-methylaniline 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:

: acetic acid-(3-iodo-5-methyl-anilide)

: 74586-54-2
3-iodo-5-methylaniline

Guidance literature:: With hydrogenchloride; In 1,4-dioxane;

Reference yield:

: 123158-78-1
1-iodo-3-methyl-5-nitrobenzene

: 74586-54-2
3-iodo-5-methylaniline

Guidance literature:: With iron(II) sulfate;

Reference yield:

: 89-62-3
4-methyl-2-nitroaniline

: 74586-54-2
3-iodo-5-methylaniline

Guidance literature:: Multi-step reaction with 4 steps

1: Iodine monochloride / acetic acid

2: sodium nitrite / ethanol

3: acetic acid

4: hydrogenchloride / 1,4-dioxane

With hydrogenchloride; Iodine monochloride; sodium nitrite; In 1,4-dioxane; ethanol; acetic acid;