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Home Bromides 3460-23-9
3460-23-9,MFCD00040852
Catalog No.:AA003KTF

3460-23-9 | N-(4-bromo-2-chlorophenyl)acetamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$7.00   $5.00
- +
5g
98%
in stock  
$19.00   $14.00
- +
25g
98%
in stock  
$80.00   $56.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003KTF
Chemical Name:
N-(4-bromo-2-chlorophenyl)acetamide
CAS Number:
3460-23-9
Molecular Formula:
C8H7BrClNO
Molecular Weight:
248.5043
MDL Number:
MFCD00040852
SMILES:
CC(=O)Nc1ccc(cc1Cl)Br
Properties
Properties
 
BP:
367.8°C at 760 mmHg  
Form:
Solid  
MP:
151-152°C  
Solubility:
Soluble in hot methanol (very faint turbidity).  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
176  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
2.2  

Upstream Synthesis Route

[1]IndianJournalofChemistry,SectionB:OrganicChemistryIncludingMedicinalChemistry,1987,vol.26,p.930-934

[1]Chemistry-AEuropeanJournal,2017,vol.23,#5,p.1044-1047

[2]TetrahedronLetters,2016,vol.57,#48,p.5390-5394

[3]JournalofChemicalResearch,Synopses,1997,#11,p.432-433

[4]EuropeanJournalofOrganicChemistry,2018,vol.2018,#43,p.5972-5979

[5]GazzettaChimicaItaliana,1908,vol.38II,p.22

[1]Patent:WO2006/26356,2006,A2,.Locationinpatent:Page/Pagecolumn31-32

[1]SyntheticCommunications,2012,vol.42,#24,p.3655-3663,9

[2]EuropeanJournalofOrganicChemistry,2018,vol.2018,#34,p.4748-4753

[3]Chemistry-AEuropeanJournal,2017,vol.23,#29,p.7031-7036

[4]OrganicandBiomolecularChemistry,2018,vol.16,#30,p.5433-5440

[5]JournaloftheIndianChemicalSociety,1981,vol.58,p.447-453

[6]JournaloftheChemicalSociety,1907,vol.91,p.1567

[7]JournaloftheChemicalSociety,1916,vol.109,p.96

[8]JournaloftheChemicalSociety,1923,vol.123,p.3394

[1]AdvancedSynthesisandCatalysis,2007,vol.349,#14-15,p.2286-2300

[2]OrganicandBiomolecularChemistry,2018,vol.16,#21,p.3881-3884

Downstream Synthesis Route

[1]Chemistry-AEuropeanJournal,2017,vol.23,p.1044-1047

[2]TetrahedronLetters,2016,vol.57,p.5390-5394

[3]JournalofChemicalResearch-PartS,1997,p.432-433

[4]EuropeanJournalofOrganicChemistry,2018,vol.2018,p.5972-5979

[5]GazzettaChimicaItaliana,1908,vol.38II,p.22

[1]SyntheticCommunications,2012,vol.42,p.3655-3663,9

[2]EuropeanJournalofOrganicChemistry,2018,vol.2018,p.4748-4753

[3]Chemistry-AEuropeanJournal,2017,vol.23,p.7031-7036

[4]OrganicandBiomolecularChemistry,2018,vol.16,p.5433-5440

[5]JournaloftheIndianChemicalSociety,1981,vol.58,p.447-453

[6]JournaloftheChemicalSociety,1907,vol.91,p.1567

[7]JournaloftheChemicalSociety,1916,vol.109,p.96

[8]JournaloftheChemicalSociety,1923,vol.123,p.3394

[1]JournaloftheChemicalSociety,1902,vol.81,p.494

[1]EuropeanJournalofOrganicChemistry,2018,vol.2018,p.4748-4753

[2]ChemischeBerichte,1900,vol.33,p.2399

[3]JournaloftheAmericanChemicalSociety,1928,vol.50,p.143

[1]JournaloftheChemicalSociety,1907,vol.91,p.1567

Literature
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SDS
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