1-Bromo-5-(chloromethyl)-2,3-dimethoxybenzene

Base Information

Chemical Name:1-Bromo-5-(chloromethyl)-2,3-dimethoxybenzene
CAS No.:52783-75-2
Molecular Formula:C9H10BrClO2
Molecular Weight:265.534
Hs Code.:
DSSTox Substance ID:DTXSID401251874
Mol file:52783-75-2.mol

Synonyms:1-bromo-5-(chloromethyl)-2,3-dimethoxybenzene;52783-75-2;DTXSID401251874;CCA78375;CS-0252159;EN300-59176;G26061

Suppliers and Price of 1-Bromo-5-(chloromethyl)-2,3-dimethoxybenzene

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 4 raw suppliers

Chemical Property of 1-Bromo-5-(chloromethyl)-2,3-dimethoxybenzene

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:263.95527
Heavy Atom Count:13
Complexity:157

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=C(C(=CC(=C1)CCl)Br)OC

Technology Process of 1-Bromo-5-(chloromethyl)-2,3-dimethoxybenzene

There total 4 articles about 1-Bromo-5-(chloromethyl)-2,3-dimethoxybenzene 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:

: 52783-74-1
(3-bromo-4,5-dimethoxyphenyl)methanol

: 52783-75-2
1-bromo-5-chloromethyl-2,3-dimethoxy-benzene

Guidance literature:: With hydrogenchloride; benzene;

Reference yield:

: 6948-30-7
5-bromoveratralaldehyde

: 52783-75-2
1-bromo-5-chloromethyl-2,3-dimethoxy-benzene

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous methanol. KOH

2: SOCl₂

With potassium hydroxide; thionyl chloride;