1-Chloro-3-(2,2-dibromocyclopropyl)benzene

Base Information

Chemical Name:1-Chloro-3-(2,2-dibromocyclopropyl)benzene
CAS No.:127510-49-0
Molecular Formula:C9H7Br2Cl
Molecular Weight:310.416
Hs Code.:
DSSTox Substance ID:DTXSID901268583
Nikkaji Number:J293.820K
Mol file:127510-49-0.mol

Synonyms:1-Chloro-3-(2,2-dibromocyclopropyl)benzene;DTXSID901268583;1-(3-Chlorophenyl)-2,2-dibromocyclopropane;1-(3-Chlorophenyl)-2,2-dibromo-cyclopropane;1-Chloro-3-(2,2-dibromocyclopropyl)benzene #;127510-49-0

Suppliers and Price of 1-Chloro-3-(2,2-dibromocyclopropyl)benzene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-Chloro-3-(2,2-dibromocyclopropyl)benzene

Chemical Property:

XLogP3:4.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:309.85825
Heavy Atom Count:12
Complexity:181

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C(C1(Br)Br)C2=CC(=CC=C2)Cl

Technology Process of 1-Chloro-3-(2,2-dibromocyclopropyl)benzene

There total 2 articles about 1-Chloro-3-(2,2-dibromocyclopropyl)benzene 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: 85.0%

: 75-25-2
Bromoform

: 2039-85-2,26100-04-9
3-Chlorostyrene

: 127510-49-0
1-chloro-3-(2,2-dibromocyclopropyl)benzene

Guidance literature:: With N-benzyl-N,N,N-triethylammonium chloride; sodium hydroxide; In water; at 20 - 60 ℃; Inert atmosphere;
DOI:10.1002/anie.201706798

Reference yield:

: 587-04-2
m-Chlorobenzaldehyde

: 127510-49-0
1-chloro-3-(2,2-dibromocyclopropyl)benzene

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium tert-butylate / tetrahydrofuran / 1 h / 20 °C / Inert atmosphere

1.2: 20 °C / Inert atmosphere

2.1: N-benzyl-N,N,N-triethylammonium chloride; sodium hydroxide / water / 20 - 60 °C / Inert atmosphere

With potassium tert-butylate; N-benzyl-N,N,N-triethylammonium chloride; sodium hydroxide; In tetrahydrofuran; water;
DOI:10.1002/anie.201706798