90-90-4,MFCD00000103
Catalog No.:AA006THR

90-90-4 | 4-Bromobenzophenone

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
98%
in stock  
$7.00   $5.00
- +
25g
98%
in stock  
$15.00   $11.00
- +
100g
98%
in stock  
$50.00   $35.00
- +
500g
98%
in stock  
$242.00   $170.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA006THR
Chemical Name:
4-Bromobenzophenone
CAS Number:
90-90-4
Molecular Formula:
C13H9BrO
Molecular Weight:
261.1140
MDL Number:
MFCD00000103
SMILES:
Brc1ccc(cc1)C(=O)c1ccccc1
NSC Number:
59863
Properties
Properties
 
BP:
350.0°C  
Form:
Solid  
MP:
80-82 °C  
Refractive Index:
1.5130 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
213  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
4.1  

Upstream Synthesis Route

[1]CollectionofCzechoslovakChemicalCommunications,2000,vol.65,#5,p.644-650

[2]SyntheticCommunications,2004,vol.34,#3,p.479-485

[3]SyntheticCommunications,2014,vol.44,#20,p.2921-2929

[1]RecueildesTravauxChimiquesdesPays-Bas,1908,vol.27,p.334

[2]JournalofFluorineChemistry,2005,vol.126,#8,p.1191-1195

[3]JournalofSolidStateChemistry,2016,vol.233,p.303-310

[1]GreenChemistry,2015,vol.17,#7,p.3733-3736

[1]RecueildesTravauxChimiquesdesPays-Bas,1908,vol.27,p.340

[1]Patent:CN104341311,2016,B,.Locationinpatent:Paragraph0057;0058;0059

[2]Patent:CN107082753,2017,A,.Locationinpatent:Paragraph0030;0031;0032;0033;0034;0035

[3]AngewandteChemie-InternationalEdition,2018,vol.57,#29,p.8947-8952

[4]Angew.Chem.,2018,vol.130,#29,p.9085-9090,6

[5]Patent:CN106565595,2017,A,.Locationinpatent:Paragraph0028;0033;0034;0035

[6]Patent:CN108727277,2018,A,.Locationinpatent:Paragraph0008;0030-0031

[7]Patent:CN103274965,2016,B,.Locationinpatent:Paragraph0058;0059;0060;0061;062

[8]ChemicalCommunications,2012,vol.48,#77,p.9586-9588

[9]ChemPlusChem,2012,vol.77,#10,p.949-958

[10]ScienceChinaChemistry,2013,vol.56,#9,p.1213-1220

[11]DyesandPigments,2014,vol.106,p.87-93

[12]Chemistry-AEuropeanJournal,2015,vol.21,#3,p.1149-1155

[13]JournalofMaterialsChemistryC,2015,vol.3,#47,p.12328-12334

[14]JournalofMaterialsChemistryC,2017,vol.5,#10,p.2552-2558

[15]Patent:CN108250205,2018,A,.Locationinpatent:Paragraph0043;0044;0045;0052;0059

Downstream Synthesis Route

[1]BulletindelaSocieteChimiquedeFrance,1956,p.1575,1578

[1]AngewandteChemie,1989,vol.101,p.329-330

[2]ChemistryLetters,2011,vol.40,p.495-497

[3]CatalysisLetters,2019,vol.149,p.2142-2157

[4]OrganicandBiomolecularChemistry,2018,vol.16,p.5094-5096

[5]MonatsheftefurChemie,2003,vol.134,p.1365-1371

[6]NewJournalofChemistry,2017,vol.41,p.12736-12745

[7]AdvancedSynthesisandCatalysis,2015,vol.357,p.3115-3120

[8]OrganicLetters,2011,vol.13,p.98-101

[9]Organometallics,2013,vol.32,p.6631-6634

[10]JournalofOrganicChemistry,1980,vol.45,p.4126-4129

[11]GreenChemistry,2009,vol.11,p.683-685

[12]RSCAdvances,2014,vol.4,p.27955-27962

[13]ChemicalCommunications,1997,p.1119-1120

[14]JournalofMedicinalChemistry,2015,vol.58,p.8564-8572

[15]TetrahedronLetters,2004,vol.45,p.2003-2007

[16]OrganicandBiomolecularChemistry,2019,vol.17,p.6007-6014

[17]Organometallics,2019,vol.38,p.4387-4391

[18]JournalofOrganicChemistry,1993,vol.58,p.7138-7142

[19]JournaloftheAmericanChemicalSociety,1939,vol.61,p.3564

[20]JournalofOrganicChemistry,1948,vol.13,p.916,920

[21]JournaloftheAmericanChemicalSociety,1929,vol.51,p.3382

[22]RecueildesTravauxChimiquesdesPays-Bas,1908,vol.27,p.340

[23]RecueildesTravauxChimiquesdesPays-Bas,1908,vol.27,p.340

[24]RecueildesTravauxChimiquesdesPays-Bas,1910,vol.29,p.153

[25]RecueildesTravauxChimiquesdesPays-Bas,1919,vol.38,p.121

[26]ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1945,vol.220,p.460

[27]JournalofOrganicChemistry,1967,vol.32,p.2692-2695

[28]JournaloftheChemicalSociety.PerkintransactionsII,1983,p.949-954

[29]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,1981,vol.20,p.998-1001

[30]JournalofOrganicChemistry,1993,vol.58,p.5907-5914

[31]CanadianJournalofChemistry,1998,vol.76,p.919-928

[32]BioorganicandMedicinalChemistryLetters,2004,vol.14,p.3691-3695

[33]OrganicLetters,2002,vol.4,p.4297-4300

[34]Pharmazie,2007,vol.62,p.174-178

[35]OrganicLetters,2007,vol.9,p.2027-2030

[36]EuropeanJournalofOrganicChemistry,2007,p.4642-4645

[37]Lettersindrugdesignanddiscovery,2010,vol.7,p.661-664

[38]ChemicalCommunications,2015,vol.51,p.15106-15109

[39]JournaloftheAmericanChemicalSociety,2016,vol.138,p.6940-6943

[40]JournalofChemistry,2016,vol.2016

[41]JournalofOrganometallicChemistry,2018,vol.876,p.57-65

[42]Patent:WO2004/22526,2004,A1.Locationinpatent:Page85-86

[43]DaltonTransactions,2019,vol.48,p.11838-11847

[1]Diss.<Univ.Berlin1933>S.31,35,

[1]JournaloftheAmericanChemicalSociety,1929,vol.51,p.3382

[1]OrganicPreparationsandProceduresInternational,1995,vol.27,p.703-706

[2]AsianJournalofChemistry,2013,vol.25,p.3307-3312

[3]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2005,vol.44,p.577-580

[4]TetrahedronLetters,2008,vol.49,p.5336-5338

[5]BulletinoftheChemicalSocietyofJapan,1989,vol.62,p.4069-4071

[6]BulletinoftheChemicalSocietyofJapan,1990,vol.63,p.2433-2434

[7]TetrahedronLetters,1997,vol.38,p.6925-6928

[8]ChemPlusChem,2012,vol.77,p.865-871

[9]CollectionofCzechoslovakChemicalCommunications,2012,vol.77,p.865-871

[10]Tetrahedron,2014,vol.70,p.2431-2438

[11]OrganicPreparationsandProceduresInternational,2013,vol.45,p.241-245

[12]Molecularcatalysis,2019,vol.469,p.27-39

[13]MonatsheftefurChemie,2017,vol.148,p.381-386

[14]ChemicalandPharmaceuticalBulletin,2017,vol.65,p.801-804

[15]ChemistryLetters,2011,vol.40,p.495-497

[16]SyntheticCommunications,2014,vol.44,p.800-806

[17]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1983,vol.22,p.413-414

[18]JournaloftheChemicalSociety.PerkintransactionsII,1983,p.949-954

[19]ZeitschriftfurPhysikalischeChemie(Leipzig),1987,vol.268,p.502-506

[20]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,1981,vol.20,p.998-1001

[21]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,1984,vol.23,p.389-391

[22]JournalofPhysicalOrganicChemistry,1997,vol.10,p.159-166

[23]InternationalJournalofChemicalKinetics,1997,vol.29,p.773-780

[24]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1997,vol.36,p.333-338

[25]AngewandteChemie-InternationalEdition,2007,vol.46,p.7210-7213

[26]JournaloftheIndianChemicalSociety,2009,vol.86,p.481-484

[27]Chemistry-AEuropeanJournal,2013,vol.19,p.5542-5545

[28]RSCAdvances,2014,vol.4,p.6597-6601

[29]CatalysisCommunications,2013,vol.40,p.27-31

Literature

Title: (E)-1-(4-Bromo-phen-yl)-2-(4-tert-butyl-phen-yl)-1-phenyl-ethene.

Journal: Acta crystallographica. Section E, Structure reports online 20080201

Title: Polymorphism of 4-bromobenzophenone.

Journal: Acta crystallographica. Section B, Structural science 20070401

Title: Synthesis of photoactivatable analogues of lysophosphatidic acid and covalent labeling of plasma proteins.

Journal: The Journal of organic chemistry 20060120

Title: In situ electrochemical-NMR spectroscopy. Reduction of aromatic halides.

Journal: Analytical chemistry 20040315

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SDS
Tags:90-90-4 Molecular Formula|90-90-4 MDL|90-90-4 SMILES|90-90-4 4-Bromobenzophenone
Catalog No.: AA006THR
90-90-4,MFCD00000103
90-90-4 | 4-Bromobenzophenone
Pack Size: 10g
Purity: 98%
in stock
$7.00 $5.00
Pack Size: 25g
Purity: 98%
in stock
$15.00 $11.00
Pack Size: 100g
Purity: 98%
in stock
$50.00 $35.00
Pack Size: 500g
Purity: 98%
in stock
$242.00 $170.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA006THR
Chemical Name: 4-Bromobenzophenone
CAS Number: 90-90-4
Molecular Formula: C13H9BrO
Molecular Weight: 261.1140
MDL Number: MFCD00000103
SMILES: Brc1ccc(cc1)C(=O)c1ccccc1
NSC Number: 59863
Properties
BP: 350.0°C  
Form: Solid  
MP: 80-82 °C  
Refractive Index: 1.5130 (estimate)  
Storage: Keep in dry area;Room Temperature;  
Complexity: 213  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 4.1  
Upstream Synthesis Route
108-86-1    98-88-4    90-90-4    13047-06-8    1016-77-9 

[1]CollectionofCzechoslovakChemicalCommunications,2000,vol.65,#5,p.644-650

[2]SyntheticCommunications,2004,vol.34,#3,p.479-485

[3]SyntheticCommunications,2014,vol.44,#20,p.2921-2929

108-86-1    98-88-4    90-90-4    13047-06-8 

[1]RecueildesTravauxChimiquesdesPays-Bas,1908,vol.27,p.334

[2]JournalofFluorineChemistry,2005,vol.126,#8,p.1191-1195

[3]JournalofSolidStateChemistry,2016,vol.233,p.303-310

108-86-1    201230-82-2    369-57-3    90-90-4    13047-06-8 

[1]GreenChemistry,2015,vol.17,#7,p.3733-3736

7446-70-0    108-86-1    98-88-4    90-90-4    13047-06-8 

[1]RecueildesTravauxChimiquesdesPays-Bas,1908,vol.27,p.340

101-81-5    90-90-4    34699-28-0 

[1]Patent:CN104341311,2016,B,.Locationinpatent:Paragraph0057;0058;0059

[2]Patent:CN107082753,2017,A,.Locationinpatent:Paragraph0030;0031;0032;0033;0034;0035

[3]AngewandteChemie-InternationalEdition,2018,vol.57,#29,p.8947-8952

[4]Angew.Chem.,2018,vol.130,#29,p.9085-9090,6

[5]Patent:CN106565595,2017,A,.Locationinpatent:Paragraph0028;0033;0034;0035

[6]Patent:CN108727277,2018,A,.Locationinpatent:Paragraph0008;0030-0031

[7]Patent:CN103274965,2016,B,.Locationinpatent:Paragraph0058;0059;0060;0061;062

[8]ChemicalCommunications,2012,vol.48,#77,p.9586-9588

[9]ChemPlusChem,2012,vol.77,#10,p.949-958

[10]ScienceChinaChemistry,2013,vol.56,#9,p.1213-1220

[11]DyesandPigments,2014,vol.106,p.87-93

[12]Chemistry-AEuropeanJournal,2015,vol.21,#3,p.1149-1155

[13]JournalofMaterialsChemistryC,2015,vol.3,#47,p.12328-12334

[14]JournalofMaterialsChemistryC,2017,vol.5,#10,p.2552-2558

[15]Patent:CN108250205,2018,A,.Locationinpatent:Paragraph0043;0044;0045;0052;0059

Downstream Synthesis Route
7341-96-0    90-90-4    132568-80-0 

[1]BulletindelaSocieteChimiquedeFrance,1956,p.1575,1578

90-90-4    29334-16-5 

[1]AngewandteChemie,1989,vol.101,p.329-330

[2]ChemistryLetters,2011,vol.40,p.495-497

[3]CatalysisLetters,2019,vol.149,p.2142-2157

[4]OrganicandBiomolecularChemistry,2018,vol.16,p.5094-5096

[5]MonatsheftefurChemie,2003,vol.134,p.1365-1371

[6]NewJournalofChemistry,2017,vol.41,p.12736-12745

[7]AdvancedSynthesisandCatalysis,2015,vol.357,p.3115-3120

[8]OrganicLetters,2011,vol.13,p.98-101

[9]Organometallics,2013,vol.32,p.6631-6634

[10]JournalofOrganicChemistry,1980,vol.45,p.4126-4129

[11]GreenChemistry,2009,vol.11,p.683-685

[12]RSCAdvances,2014,vol.4,p.27955-27962

[13]ChemicalCommunications,1997,p.1119-1120

[14]JournalofMedicinalChemistry,2015,vol.58,p.8564-8572

[15]TetrahedronLetters,2004,vol.45,p.2003-2007

[16]OrganicandBiomolecularChemistry,2019,vol.17,p.6007-6014

[17]Organometallics,2019,vol.38,p.4387-4391

[18]JournalofOrganicChemistry,1993,vol.58,p.7138-7142

[19]JournaloftheAmericanChemicalSociety,1939,vol.61,p.3564

[20]JournalofOrganicChemistry,1948,vol.13,p.916,920

[21]JournaloftheAmericanChemicalSociety,1929,vol.51,p.3382

[22]RecueildesTravauxChimiquesdesPays-Bas,1908,vol.27,p.340

[23]RecueildesTravauxChimiquesdesPays-Bas,1908,vol.27,p.340

[24]RecueildesTravauxChimiquesdesPays-Bas,1910,vol.29,p.153

[25]RecueildesTravauxChimiquesdesPays-Bas,1919,vol.38,p.121

[26]ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1945,vol.220,p.460

[27]JournalofOrganicChemistry,1967,vol.32,p.2692-2695

[28]JournaloftheChemicalSociety.PerkintransactionsII,1983,p.949-954

[29]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,1981,vol.20,p.998-1001

[30]JournalofOrganicChemistry,1993,vol.58,p.5907-5914

[31]CanadianJournalofChemistry,1998,vol.76,p.919-928

[32]BioorganicandMedicinalChemistryLetters,2004,vol.14,p.3691-3695

[33]OrganicLetters,2002,vol.4,p.4297-4300

[34]Pharmazie,2007,vol.62,p.174-178

[35]OrganicLetters,2007,vol.9,p.2027-2030

[36]EuropeanJournalofOrganicChemistry,2007,p.4642-4645

[37]Lettersindrugdesignanddiscovery,2010,vol.7,p.661-664

[38]ChemicalCommunications,2015,vol.51,p.15106-15109

[39]JournaloftheAmericanChemicalSociety,2016,vol.138,p.6940-6943

[40]JournalofChemistry,2016,vol.2016

[41]JournalofOrganometallicChemistry,2018,vol.876,p.57-65

[42]Patent:WO2004/22526,2004,A1.Locationinpatent:Page85-86

[43]DaltonTransactions,2019,vol.48,p.11838-11847

5472-32-2    103-73-1    29334-16-5    90-90-4 

[1]Diss.<Univ.Berlin1933>S.31,35,

90-90-4    927-77-5    71-43-2    29334-16-5 

[1]JournaloftheAmericanChemicalSociety,1929,vol.51,p.3382

29334-16-5    90-90-4 

[1]OrganicPreparationsandProceduresInternational,1995,vol.27,p.703-706

[2]AsianJournalofChemistry,2013,vol.25,p.3307-3312

[3]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2005,vol.44,p.577-580

[4]TetrahedronLetters,2008,vol.49,p.5336-5338

[5]BulletinoftheChemicalSocietyofJapan,1989,vol.62,p.4069-4071

[6]BulletinoftheChemicalSocietyofJapan,1990,vol.63,p.2433-2434

[7]TetrahedronLetters,1997,vol.38,p.6925-6928

[8]ChemPlusChem,2012,vol.77,p.865-871

[9]CollectionofCzechoslovakChemicalCommunications,2012,vol.77,p.865-871

[10]Tetrahedron,2014,vol.70,p.2431-2438

[11]OrganicPreparationsandProceduresInternational,2013,vol.45,p.241-245

[12]Molecularcatalysis,2019,vol.469,p.27-39

[13]MonatsheftefurChemie,2017,vol.148,p.381-386

[14]ChemicalandPharmaceuticalBulletin,2017,vol.65,p.801-804

[15]ChemistryLetters,2011,vol.40,p.495-497

[16]SyntheticCommunications,2014,vol.44,p.800-806

[17]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1983,vol.22,p.413-414

[18]JournaloftheChemicalSociety.PerkintransactionsII,1983,p.949-954

[19]ZeitschriftfurPhysikalischeChemie(Leipzig),1987,vol.268,p.502-506

[20]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,1981,vol.20,p.998-1001

[21]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,1984,vol.23,p.389-391

[22]JournalofPhysicalOrganicChemistry,1997,vol.10,p.159-166

[23]InternationalJournalofChemicalKinetics,1997,vol.29,p.773-780

[24]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1997,vol.36,p.333-338

[25]AngewandteChemie-InternationalEdition,2007,vol.46,p.7210-7213

[26]JournaloftheIndianChemicalSociety,2009,vol.86,p.481-484

[27]Chemistry-AEuropeanJournal,2013,vol.19,p.5542-5545

[28]RSCAdvances,2014,vol.4,p.6597-6601

[29]CatalysisCommunications,2013,vol.40,p.27-31

Literature fold

Title: (E)-1-(4-Bromo-phen-yl)-2-(4-tert-butyl-phen-yl)-1-phenyl-ethene.

Journal: Acta crystallographica. Section E, Structure reports online20080201

Title: Polymorphism of 4-bromobenzophenone.

Journal: Acta crystallographica. Section B, Structural science20070401

Title: Synthesis of photoactivatable analogues of lysophosphatidic acid and covalent labeling of plasma proteins.

Journal: The Journal of organic chemistry20060120

Title: In situ electrochemical-NMR spectroscopy. Reduction of aromatic halides.

Journal: Analytical chemistry20040315

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