2-(1-Bromoethyl)-1-methyl-4-nitrobenzene

Base Information

Chemical Name:2-(1-Bromoethyl)-1-methyl-4-nitrobenzene
CAS No.:58966-28-2
Molecular Formula:C₉H₁₀BrNO₂
Molecular Weight:244.088
Hs Code.:
DSSTox Substance ID:DTXSID801273812

Synonyms:2-(1-Bromoethyl)-1-methyl-4-nitrobenzene;58966-28-2;SCHEMBL16971138;DTXSID801273812

Suppliers and Price of 2-(1-Bromoethyl)-1-methyl-4-nitrobenzene

Supply Marketing:

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

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Chemical Property of 2-(1-Bromoethyl)-1-methyl-4-nitrobenzene

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:242.98949
Heavy Atom Count:13
Complexity:193

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=C(C=C(C=C1)[N+](=O)[O-])C(C)Br

Technology Process of 2-(1-Bromoethyl)-1-methyl-4-nitrobenzene

There total 3 articles about 2-(1-Bromoethyl)-1-methyl-4-nitrobenzene 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: 96.0%

: 58966-28-2
2-(1-bromoethyl)-1-methyl-4-nitro-benzene

Guidance literature:

Reference yield:

: 58966-27-1
2'-methyl-5'-nitro-acetophenone

: 58966-28-2
2-(1-bromoethyl)-1-methyl-4-nitro-benzene

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaBH₄ / methanol

2: HBr / benzene

With sodium tetrahydroborate; hydrogen bromide; In methanol; benzene;

Reference yield:

: 16634-91-6
2-methyl-5-nitro-benzaldehyde

: 58966-28-2
2-(1-bromoethyl)-1-methyl-4-nitro-benzene

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether

2: hydrogen bromide / acetic acid

With hydrogen bromide; In diethyl ether; acetic acid;