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N-(3-Bromo-5-ethylphenyl)acetamide

Base Information
  • Chemical Name:N-(3-Bromo-5-ethylphenyl)acetamide
  • CAS No.:123158-67-8
  • Molecular Formula:C10H12BrNO
  • Molecular Weight:242.115
  • Hs Code.:
  • DSSTox Substance ID:DTXSID301295908
  • Mol file:123158-67-8.mol
N-(3-Bromo-5-ethylphenyl)acetamide

Synonyms:N-(3-Bromo-5-ethylphenyl)acetamide;123158-67-8;Acetamide, N-(3-bromo-5-ethylphenyl)-;SCHEMBL9452430;DTXSID301295908;YEA15867;AKOS024462990;DS-3206;DB-172618;CS-0152521;C71905

Suppliers and Price of N-(3-Bromo-5-ethylphenyl)acetamide
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
  • Matrix Scientific
  • N-(3-Bromo-5-ethylphenyl)acetamide >95%
  • 1g
  • $ 504.00
  • Crysdot
  • N-(3-Bromo-5-ethylphenyl)acetamide 95+%
  • 5g
  • $ 624.00
  • Ambeed
  • N-(3-Bromo-5-ethylphenyl)acetamide 95%
  • 5g
  • $ 784.00
  • Ambeed
  • N-(3-Bromo-5-ethylphenyl)acetamide 95%
  • 1g
  • $ 181.00
  • Ambeed
  • N-(3-Bromo-5-ethylphenyl)acetamide 95%
  • 250mg
  • $ 100.00
  • Abosyn
  • N-(3-Bromo-5-ethylphenyl)acetamide 95-98%
  • 1g
  • $ 250.00
Total 8 raw suppliers
Chemical Property of N-(3-Bromo-5-ethylphenyl)acetamide
Chemical Property:
  • PSA:29.10000 
  • LogP:3.04290 
  • Storage Temp.:Sealed in dry,Room Temperature 
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:2
  • Exact Mass:241.01023
  • Heavy Atom Count:13
  • Complexity:184
Purity/Quality:

97% *data from raw suppliers

N-(3-Bromo-5-ethylphenyl)acetamide >95% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC1=CC(=CC(=C1)Br)NC(=O)C
Technology Process of N-(3-Bromo-5-ethylphenyl)acetamide

There total 9 articles about N-(3-Bromo-5-ethylphenyl)acetamide 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:
Guidance literature:
Multi-step reaction with 5 steps
1: acetic acid; sulfuric acid; nitric acid
2: aqueous sulfuric acid
3: ethanolic sulfuric acid; aqueous sodium nitrite solution
4: tin; aqueous hydrochloric acid
With hydrogenchloride; tin; sulfuric acid; nitric acid; acetic acid; sodium nitrite;
Guidance literature:
Multi-step reaction with 8 steps
1: acetic acid; sulfuric acid; nitric acid
2: aq.-ethanolic hydrochloric acid
3: ethanol; sulfuric acid; sodium nitrite / und Erhitzen des Reaktionsprodukts mit Zinn(II)-chlorid und wss.Salzsaeure und Behandeln des erhaltenen Amins mit Acetanhydrid
4: acetic acid; sulfuric acid; nitric acid
5: aqueous sulfuric acid
6: ethanolic sulfuric acid; aqueous sodium nitrite solution
7: tin; aqueous hydrochloric acid
With hydrogenchloride; tin; ethanol; sulfuric acid; nitric acid; acetic acid; sodium nitrite;
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