1,3-dibromo-2-chloro-5-methoxybenzene

Base Information

Chemical Name:1,3-dibromo-2-chloro-5-methoxybenzene
CAS No.:174913-47-4
Molecular Formula:C₇H₅Br₂ClO
Molecular Weight:300.377
Hs Code.:

Synonyms:1,3-dibromo-2-chloro-5-methoxybenzene

Suppliers and Price of 1,3-dibromo-2-chloro-5-methoxybenzene

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
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price

Crysdot
1,3-Dibromo-2-chloro-5-methoxybenzene 95+%
5g
$ 585.00

Total 1 raw suppliers

Chemical Property of 1,3-dibromo-2-chloro-5-methoxybenzene

Chemical Property:

Purity/Quality:: 1,3-Dibromo-2-chloro-5-methoxybenzene 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1,3-dibromo-2-chloro-5-methoxybenzene

There total 9 articles about 1,3-dibromo-2-chloro-5-methoxybenzene 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: 95.0%

: 74137-36-3
3,5-dibromoanisole

: 174913-47-4
1,3-dibromo-2-chloro-5-methoxybenzene

Guidance literature:: With N-chloro-succinimide; In acetonitrile; at 86.9 ℃; for 40h;

Reference yield: 52.0%

: 95970-05-1
2,6-dibromo-4-methoxyaniline

: 174913-47-4
1,3-dibromo-2-chloro-5-methoxybenzene

Guidance literature:: 2,6-dibromo-4-methoxyaniline; With hydrogenchloride; sodium nitrite; at 0 ℃;

With copper(l) chloride; Further stages.;
DOI:10.1021/ja074778x

Reference yield:

: 106-48-9,82344-39-6
4-chloro-phenol

: 174913-47-4
1,3-dibromo-2-chloro-5-methoxybenzene

Guidance literature:: Multi-step reaction with 5 steps

1: alkaline solution

2: nitric acid

3: tin; concentrated hydrochloric acid

4: glacial acetic acid; bromine / unter Kuehlung

5: alcohol; sulfuric acid / Diazotization

With hydrogenchloride; tin; ethanol; alkaline solution; sulfuric acid; bromine; nitric acid; acetic acid;
DOI:10.1017/S1092852900017430