Home Bromides 1779-51-7
1779-51-7,MFCD00011855
Catalog No.:AA0025J3

1779-51-7 | Phosphonium, butyltriphenyl-, bromide (1:1)

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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
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  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0025J3
Chemical Name:
Phosphonium, butyltriphenyl-, bromide (1:1)
CAS Number:
1779-51-7
Molecular Formula:
C22H24BrP
Molecular Weight:
399.3037
MDL Number:
MFCD00011855
SMILES:
CCCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
NSC Number:
59684
Properties
Properties
 
Form:
Solid  
MP:
240-243 °C(lit.)  
Stability:
Hygroscopic  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
273  
Covalently-Bonded Unit Count:
2  
Heavy Atom Count:
24  
Hydrogen Bond Acceptor Count:
1  
Rotatable Bond Count:
6  

Upstream Synthesis Route

[1]Patent:JP6136589,2017,B2,.Locationinpatent:Paragraph0102-0104

[2]ActaChimicaHungarica,1987,vol.124,#5,p.737-748

[3]JournalofFluorineChemistry,2002,vol.113,#2,p.177-183

[4]Pharmazie,1999,vol.54,#1,p.26-30

[5]SyntheticCommunications,1981,vol.11,#2,p.125-132

[6]JournalofOrganicChemistry,1984,vol.49,#22,p.4293-4295

[7]TetrahedronLetters,2017,vol.58,#33,p.3311-3315

[8]AdvancedSynthesisandCatalysis,2009,vol.351,#3,p.375-378

[9]JournalofPolymerScience,PartA:PolymerChemistry,2016,vol.54,#8,p.1088-1097

[10]EuropeanJournalofOrganicChemistry,2008,#10,p.1677-1679

[11]OrganicLetters,2012,vol.14,#22,p.5784-5787

[12]JournalofOrganometallicChemistry,1996,vol.507,#1-2,p.53-63

[13]BulletinoftheChemicalSocietyofJapan,1996,vol.69,#3,p.655-664

[14]JournalofOrganometallicChemistry,1999,vol.580,#2,p.282-289

[15]IndianJournalofChemistry,SectionA:Inorganic,Bio-inorganic,Physical,Theoretical&AnalyticalChemistry,1991,vol.30,#11,p.929-935

[16]JournaloftheAmericanChemicalSociety,1960,vol.82,p.3919-3924

[17]JournaloftheAmericanChemicalSociety,1958,vol.80,p.4386

[18]YukiGoseiKagakuKyokaishi,1950,vol.8,#9,p.27,30

[19]Chem.Abstr.,1953,p.814

[20]BulletinoftheChemicalSocietyofJapan,1954,vol.22,p.509,511

[21]JustusLiebigsAnnalenderChemie,1961,vol.646,p.65-77

[22]JournaloftheChemicalSociety,1961,p.539-542

[23]BulletindelaSocieteChimiquedeFrance,1972,p.3930-3936

[24]Tetrahedron,1986,vol.42,#14,p.3813-3824

[25]Tetrahedron,1988,vol.44,#4,p.1057-1072

[26]SyntheticCommunications,1982,vol.12,#2,p.107-112

[27]ActaChimicaAcademiaeScientiarumHungaricae,1982,vol.110,#2,p.153-162

[28]JournalofSolutionChemistry,1980,vol.9,p.809-818

[29]IndianJournalofChemistry,SectionA:Inorganic,Bio-inorganic,Physical,Theoretical&AnalyticalChemistry,1991,vol.30,#11,p.929-935

[30]J.Gen.Chem.USSR(Engl.Transl.),1984,vol.54,#11,p.2279-2281

[31]ZhurnalObshcheiKhimii,1984,vol.54,#11,p.2550-2553

[32]AustralianJournalofChemistry,1997,vol.50,#12,p.1129-1135

[33]ChemistryofNaturalCompounds,2001,vol.37,#3,p.282-284

[34]CarbohydrateResearch,2012,vol.358,p.23-30

[35]ChemicalCommunications,2015,vol.51,#43,p.9002-9005

[36]OrganicLetters,2016,vol.18,#3,p.504-507

[37]OrganicandBiomolecularChemistry,2016,vol.14,#35,p.8356-8366

[38]Patent:US2016/297829,2016,A1,.Locationinpatent:Paragraph0159;0160

[1]Phosphorus,SulfurandSiliconandtheRelatedElements,1990,vol.48,#1-4,p.279-280

[1]PhosphorusandSulfurandtheRelatedElements,1987,vol.29,p.111-114

[1]PhosphorusandSulfurandtheRelatedElements,1987,vol.29,p.111-114

[1]BulletinoftheChemicalSocietyofJapan,

[2]BulletinoftheChemicalSocietyofJapan,1954,vol.27,p.509-515

[3],GmelinHandbook:Ni:MVol.C2,8.18.1,page1041-1052,

Downstream Synthesis Route

[1]Patent:JP6136589,2017,B2.Locationinpatent:Paragraph0102-0104

[2]ActaChimicaHungarica,1987,vol.124,p.737-748

[3]JournalofFluorineChemistry,2002,vol.113,p.177-183

[4]Pharmazie,1999,vol.54,p.26-30

[5]JournaloftheAmericanChemicalSociety,2019,vol.141,p.12760-12769

[6]Patent:CN110003273,2019,A.Locationinpatent:Paragraph0041-0044

[7]SyntheticCommunications,1981,vol.11,p.125-132

[8]JournalofOrganicChemistry,1984,vol.49,p.4293-4295

[9]TetrahedronLetters,2017,vol.58,p.3311-3315

[10]AdvancedSynthesisandCatalysis,2009,vol.351,p.375-378

[11]JournalofPolymerScience,PartA:PolymerChemistry,2016,vol.54,p.1088-1097

[12]EuropeanJournalofOrganicChemistry,2008,p.1677-1679

[13]OrganicLetters,2012,vol.14,p.5784-5787

[14]AngewandteChemie-InternationalEdition,2019,vol.58,p.18552-18556    Angew.Chem.,2019,vol.131,p.18724-18729,6

[15]JournalofOrganometallicChemistry,1996,vol.507,p.53-63

[16]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,1991,vol.30,p.929-935

[17]JournaloftheAmericanChemicalSociety,1960,vol.82,p.3919-3924

[18]JustusLiebigsAnnalenderChemie,1961,vol.646,p.65-77

[19]JournaloftheChemicalSociety,1961,p.539-542

[20]BulletindelaSocieteChimiquedeFrance,1972,p.3930-3936

[21]Tetrahedron,1986,vol.42,p.3813-3824

[22]Tetrahedron,1988,vol.44,p.1057-1072

[23]ActaChimicaAcademiaeScientiarumHungaricae,1982,vol.110,p.153-162

[24]JournalofSolutionChemistry,1980,vol.9,p.809-818

[25]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,1991,vol.30,p.929-935

[26]JournalofgeneralchemistryoftheUSSR,1984,vol.54,p.2279-2281    ZhurnalObshcheiKhimii,1984,vol.54,p.2550-2553

[27]AustralianJournalofChemistry,1997,vol.50,p.1129-1135

[28]ChemistryofNaturalCompounds,2001,vol.37,p.282-284

[29]CarbohydrateResearch,2012,vol.358,p.23-30

[30]ChemicalCommunications,2015,vol.51,p.9002-9005

[31]OrganicLetters,2016,vol.18,p.504-507

[32]OrganicandBiomolecularChemistry,2016,vol.14,p.8356-8366

[33]Patent:US2016/297829,2016,A1.Locationinpatent:Paragraph0159;0160

[34]JournaloftheAmericanChemicalSociety,2018,vol.140,p.11317-11324

[35]AdvancedMaterials,2020,vol.32

[1]Tetrahedron,1968,vol.24,p.2419-2423

[1]TetrahedronLetters,1980,vol.21,p.4831-4834

[2]Chem,2020,vol.6,p.675-688

344-07-0    1779-51-7    13371-17-0   
1-(4-Chloro-2,3,5,6-tetrafluoro-phenyl)-butylidene-triphenyl-λ5-phosphane 

[1]Shen,Yanchang;Qiu,Weiming[JournalofFluorineChemistry,1988,vol.38,p.175-182]

[1]Tetrahedron,1988,vol.44,p.1057-1072

Literature

Title: Tandem mass spectrometric characterization of thiol peptides modified by the chemoselective cationic sulfhydryl reagent (4-iodobutyl)triphenylphosphonium--effects of a cationic thiol derivatization on peptide fragmentation.

Journal: Journal of the American Society for Mass Spectrometry 20111001

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Tags:1779-51-7 Molecular Formula|1779-51-7 MDL|1779-51-7 SMILES|1779-51-7 Phosphonium, butyltriphenyl-, bromide (1:1)