Home Bromides 2142-63-4
2142-63-4,MFCD00000083
Catalog No.:AA0033JV

2142-63-4 | 3'-Bromoacetophenone

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Purity
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10g
98%
in stock  
$6.00   $4.00
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25g
98%
in stock  
$13.00   $9.00
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100g
90%(GC)
in stock  
$24.00   $17.00
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500g
90%(GC)
in stock  
$78.00   $55.00
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  • 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:
AA0033JV
Chemical Name:
3'-Bromoacetophenone
CAS Number:
2142-63-4
Molecular Formula:
C8H7BrO
Molecular Weight:
199.0446
MDL Number:
MFCD00000083
SMILES:
Brc1cccc(c1)C(=O)C
NSC Number:
46620
Properties
Properties
 
BP:
255.2°C at 760 mmHg  
Form:
Liquid  
MP:
8-11 °C(lit.)  
Refractive Index:
n20/D 1.576(lit.)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
133  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
2.6  

Upstream Synthesis Route

[1]JournalofMedicinalChemistry,2006,vol.49,#6,p.1910-1915

[2]Farmaco,EdizioneScientifica,1985,vol.40,#4,p.272-284

[3]OrganicLetters,2017,vol.19,#23,p.6344-6347

[4]OrganicandBiomolecularChemistry,2018,vol.16,#25,p.4683-4687

[1]Chemistry-AnAsianJournal,2016,vol.11,#3,p.395-400

[1]RSCAdvances,2016,vol.6,#27,p.22749-22753

[1]JournalofOrganicChemistry,2012,vol.77,#7,p.3127-3133

[1]Patent:CN102898374,2016,B,.Locationinpatent:Paragraph0027-0029

[2]ChemicalCommunications,2015,vol.52,#2,p.331-334

[3]BioorganicandMedicinalChemistry,2016,vol.24,#11,p.2504-2518

[4]JournaloftheAmericanChemicalSociety,1996,vol.118,#34,p.8127-8135

Downstream Synthesis Route

[1]RecueildesTravauxChimiquesdesPays-Bas,1935,vol.54,p.813,824

[1]BulletinoftheChemicalSocietyofEthiopia,2018,vol.32,p.179-184

[2]JournalofOrganicChemistry,1937,vol.2,p.276,283

[3]Chemicalandpharmaceuticalbulletin,1968,vol.16,p.2456-2462

[4]JournalofPhysicalChemistry,1983,vol.87,p.4622-4627

[1]JournaloftheAmericanChemicalSociety,1982,vol.104,p.4173-4179

[2]Patent:US2007/254892,2007,A1.Locationinpatent:Page/Pagecolumn42

[3]ChemicalCommunications,2011,vol.47,p.3989-3991

[1]JournalofMedicinalChemistry,2006,vol.49,p.1910-1915

[2]Farmaco,EdizioneScientifica,1985,vol.40,p.272-284

[3]OrganicLetters,2017,vol.19,p.6344-6347

[4]OrganicandBiomolecularChemistry,2018,vol.16,p.4683-4687

[1]Chemistry-AnAsianJournal,2011,vol.6,p.899-908

[2]OrganicLetters,2016,vol.18,p.2938-2941

[3]OrganicLetters,2017,vol.19,p.690-693

[4]RSCAdvances,2013,vol.3,p.6747-6751

[5]DaltonTransactions,2013,vol.42,p.6513-6522

[6]Tetrahedron,2001,vol.57,p.5027-5038

[7]ChemicalCommunications,2015,vol.51,p.6123-6125

[8]AdvancedSynthesisandCatalysis,2016,vol.358,p.4006-4018

[9]TetrahedronLetters,1997,vol.38,p.375-378

[10]JournalofMolecularCatalysisA:Chemical,2012,vol.357,p.133-140

[11]TetrahedronLetters,1991,vol.32,p.7175-7178

[12]EuropeanJournalofOrganicChemistry,2013,p.5439-5444

[13]AdvancedSynthesisandCatalysis,2011,vol.353,p.1345-1352

[14]ChemCatChem,2014,vol.6,p.1368-1374

[15]SyntheticCommunications,2020,vol.50,p.1035-1045

[16]TetrahedronAsymmetry,2005,vol.16,p.2539-2549

[17]TetrahedronAsymmetry,2010,vol.21,p.566-570

[18]Chirality,2010,vol.22,p.543-547

[19]ChemicalCommunications,1998,p.2161-2162

[20]ChemicalCommunications,2003,p.2916-2917

[21]Patent:US2008/255355,2008,A1.Locationinpatent:Page/Pagecolumn8-9

[22]Patent:US2008/255355,2008,A1.Locationinpatent:Page/Pagecolumn8-9

[23]CentralEuropeanJournalofChemistry,2011,vol.9,p.175-179

[24]ChemicalCommunications,2012,vol.48,p.6286-6288

[25]AdvancedSynthesisandCatalysis,2012,vol.354,p.3250-3258

[26]InorganicChemistry,2013,vol.52,p.6193-6198

[27]GreenChemistry,2013,vol.15,p.2208-2214

[28]OrganicProcessResearchandDevelopment,2003,vol.7,p.89-94

[29]Chemistry-AEuropeanJournal,2014,vol.20,p.1515-1519

[30]ChineseChemicalLetters,2014,vol.25,p.613-616

[31]ArchivesofBiochemistryandBiophysics,2016,vol.606,p.151-156

[32]Chemistry-AEuropeanJournal,2017,vol.23,p.970-975

[33]Organometallics,2017,vol.36,p.4136-4144

[34]ChemCatChem,2018,vol.10,p.920-924

[35]Catalysisscienceandtechnology,2018,vol.8,p.2304-2311

Literature

Title: (E)-1-(3-Bromo-phen-yl)-3-(3,4-dimeth-oxy-phen-yl)prop-2-en-1-one.

Journal: Acta crystallographica. Section E, Structure reports online 20120301

Title: catena-Poly[[[(2,2'-bipyridine-κN,N')cobalt(II)]-μ-(E)-3,3'-(but-2-ene-2,3-di-yl)dibenzoato-κO,O':O'',O'''] hemihydrate].

Journal: Acta crystallographica. Section E, Structure reports online 20111101

Title: 3,5-dimethylisoxazoles act as acetyl-lysine-mimetic bromodomain ligands.

Journal: Journal of medicinal chemistry 20111013

Title: (E)-1-(2,4-Dinitro-phen-yl)-2-(2-fluoro-benzyl-idene)hydrazine.

Journal: Acta crystallographica. Section E, Structure reports online 20110501

Title: (1E)-1-(3-Bromo-phen-yl)ethanone 2,4-di-nitro-phenyl-hydrazone.

Journal: Acta crystallographica. Section E, Structure reports online 20101101

Title: (2E)-1-(3-Bromo-phen-yl)-3-(6-meth-oxy-2-naphth-yl)prop-2-en-1-one.

Journal: Acta crystallographica. Section E, Structure reports online 20101001

Title: (E)-3-(Biphenyl-4-yl)-1-(3-bromo-phen-yl)prop-2-en-1-one.

Journal: Acta crystallographica. Section E, Structure reports online 20091101

Title: (E)-1-(3-Bromo-phen-yl)-3-(4-ethoxy-phen-yl)prop-2-en-1-one.

Journal: Acta crystallographica. Section E, Structure reports online 20080701

Title: A convenient catalyst system for microwave accelerated cross-coupling of a range of aryl boronic acids with aryl chlorides.

Journal: Beilstein journal of organic chemistry 20070101

Title: New chiral ruthenium(II) catalysts containing 2,6-bis(4'-(R)-phenyloxazolin-2'-yl)pyridine (Ph-pybox) ligands for highly enantioselective transfer hydrogenation of ketones.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20040123

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Tags:2142-63-4 Molecular Formula|2142-63-4 MDL|2142-63-4 SMILES|2142-63-4 3'-Bromoacetophenone |Organic_Building_Blocks