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Home Amines 37904-72-6
37904-72-6,MFCD06409221
Catalog No.:AA00C0KH

37904-72-6 | 2-Bromo-1-(4-dimethylaminophenyl)ethanone

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$53.00   $37.00
- +
1g
95%
in stock  
$80.00   $56.00
- +
5g
95%
in stock  
$310.00   $217.00
- +
10g
95%
in stock  
$469.00   $328.00
- +
25g
95%
in stock  
$945.00   $662.00
- +
  • 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:
AA00C0KH
Chemical Name:
2-Bromo-1-(4-dimethylaminophenyl)ethanone
CAS Number:
37904-72-6
Molecular Formula:
C10H12BrNO
Molecular Weight:
242.1124
MDL Number:
MFCD06409221
SMILES:
BrCC(=O)c1ccc(cc1)N(C)C
Properties
Properties
 
BP:
330.2°C at 760 mmHg  
Form:
Solid  
MP:
89-92 °C  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
174  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
3  
XLogP3:
2.9  

Upstream Synthesis Route

[1]TetrahedronLetters,1998,vol.39,#28,p.4987-4990

[2]Patent:US2007/258887,2007,A1,.Locationinpatent:Page/Pagecolumn28;39-40

[3]ChemicalCommunications,2016,vol.52,#90,p.13277-13280

[4]BioorganicandMedicinalChemistryLetters,2011,vol.21,#10,p.2966-2968

[5]ACSMedicinalChemistryLetters,2013,vol.4,#7,p.596-600

[6]Patent:US2014/88306,2014,A1,.Locationinpatent:Paragraph0050-0051

[7]Patent:WO2015/200619,,A1,.Locationinpatent:Paragraph0272

[7]Patent:,2015,,.Locationinpatent:Paragraph0272

[9]JournalofLabelledCompoundsandRadiopharmaceuticals,2001,vol.44,p.S29-S32

[10]JournaloftheChemicalSociety,DaltonTransactions,2002,vol.2,#1,p.48-54

[11]JournaloftheAmericanChemicalSociety,2009,vol.131,#46,p.16663-16665

[12]Patent:WO2013/82508,2013,A1,.Locationinpatent:Sheet9/10

[1]EuropeanJournalofOrganicChemistry,2007,#29,p.4831-4836

[2]JournalofOrganicChemistry,2018,vol.83,#3,p.1095-1105

[3]OrganicandBiomolecularChemistry,2016,vol.14,#30,p.7268-7274

[4]YakugakuZasshi,1955,vol.75,p.54

[5]Chem.Abstr.,1956,p.864

[6]JournaloftheChemicalSociety,DaltonTransactions,2002,vol.2,#1,p.48-54

[7]JournalofLabelledCompoundsandRadiopharmaceuticals,2001,vol.44,p.S29-S32

[8]TetrahedronLetters,1998,vol.39,#28,p.4987-4990

[9]BioorganicandMedicinalChemistryLetters,2011,vol.21,#10,p.2966-2968

[10]BioorganicandMedicinalChemistryLetters,2011,vol.21,#14,p.4193-4196

[11]ACSMedicinalChemistryLetters,2013,vol.4,#7,p.596-600

[12]Patent:WO2013/82508,2013,A1,

[13]Patent:US2014/88306,2014,A1,

[14]Patent:WO2015/200619,,A1,

[14]Patent:,2015,,

[1]TetrahedronLetters,1998,vol.39,#28,p.4987-4990

Downstream Synthesis Route

[1]Chemicalandpharmaceuticalbulletin,1977,vol.25,p.3370-3375

[1]Synthesis,1990,p.707-712

[1]Synthesis,1990,p.795-798

[1]Synthesis,1990,p.707-712

[1]Synthesis,1990,p.707-712

Literature
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SDS
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