Catalog No.:AA003AWA

59159-39-6 | (tert-Butoxycarbonylmethyl)triphenylphosphonium bromide

Name: Name:(tert-Butoxycarbonylmethyl)triphenylphosphonium bromide
Brand: AABLOCKS
SKU: AA003AWA
Availability: InStock
Rating: 90 (10 reviews)

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Quantity

97%

in stock

$8.00 $6.00

- +

97%

in stock

$13.00 $9.00

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25g

95%

in stock

$45.00 $32.00

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100g

97%

in stock

$51.00 $36.00

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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
Request for Quotation
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA003AWA

Chemical Name:

(tert-Butoxycarbonylmethyl)triphenylphosphonium bromide

CAS Number:

59159-39-6

Molecular Formula:

C24H26BrO2P

Molecular Weight:

457.3398

MDL Number:

MFCD00075527

SMILES:

O=C(C[P+](c1ccccc1)(c1ccccc1)c1ccccc1)OC(C)(C)C.[Br-]

NSC Number:

82468

Properties

Form:

Solid

MP:

178 °C (dec.)(lit.)

Storage:

Inert atmosphere;Room Temperature;

Computed Properties

Complexity:

418

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Upstream Synthesis Route

5292-43-3

603-35-0

59159-39-6

[1]Patent:US2007/265243,2007,A1,.Locationinpatent:Page/Pagecolumn4

[2]BioorganicandMedicinalChemistry,2001,vol.9,#1,p.199-209

[3]Phosphorus,SulfurandSiliconandtheRelatedElements,2008,vol.183,#5,p.1188-1208

[4]Patent:US2007/43088,2007,A1,.Locationinpatent:Page/Pagecolumn5

[5]OrganicProcessResearchandDevelopment,2009,vol.13,#4,p.710-715

[6]Heterocycles,2007,vol.73,#C,p.751-768

[7]Bioscience,BiotechnologyandBiochemistry,2010,vol.74,#4,p.741-745

[8]JournalofOrganicChemistry,2008,vol.73,#23,p.9465-9468

[9]JournaloftheAmericanChemicalSociety,1979,vol.101,p.6023-6027

[10]JournalofOrganicChemistry,1988,vol.53,#23,p.5558-5562

[11]ChemischeBerichte,1986,vol.119,#4,p.1196-1207

[12]AdvancedSynthesisandCatalysis,2018,vol.360,#7,p.1510-1516

59159-39-6

626-34-6

643-79-8

103890-78-4

[1]Patent:US2007/43088,2007,A1,.Locationinpatent:Page/Pagecolumn6

Downstream Synthesis Route

3298-40-6

59159-39-6

41502-69-6

[1]JournaloftheAmericanChemicalSociety,1979,vol.101,p.6023-6027

59159-39-6

91635-03-9

94029-65-9

[1]ChemischeBerichte,1964,vol.97,p.1846-1856

5292-43-3

603-35-0

59159-39-6

[1]Patent:US2007/265243,2007,A1.Locationinpatent:Page/Pagecolumn4

[2]BioorganicandMedicinalChemistry,2001,vol.9,p.199-209

[3]Phosphorus,SulfurandSiliconandtheRelatedElements,2008,vol.183,p.1188-1208

[4]Patent:US2007/43088,2007,A1.Locationinpatent:Page/Pagecolumn5

[5]OrganicProcessResearchandDevelopment,2009,vol.13,p.710-715

[6]Heterocycles,2007,vol.73,p.751-768

[7]Bioscience,BiotechnologyandBiochemistry,2010,vol.74,p.741-745

[8]JournalofOrganicChemistry,2008,vol.73,p.9465-9468

[9]JournaloftheAmericanChemicalSociety,1979,vol.101,p.6023-6027

[10]JournalofOrganicChemistry,1988,vol.53,p.5558-5562

[11]ChemischeBerichte,1986,vol.119,p.1196-1207

[12]AdvancedSynthesisandCatalysis,2018,vol.360,p.1510-1516

[13]TetrahedronLetters,2019,vol.60,p.1885-1890

[14]OrganicLetters,2019,vol.21,p.7055-7059

59159-39-6

2-Azido-3-ethylbenzthiazolium-tetrafluoroborat

2-Amino-3-ethylbenzthiazoliumbromid

<Diazo(tert-butoxycarbonyl)-methyl>-triphenylphosphonium-tetrafluoroborat

[1]LiebigsAnnalenderChemie,1981,p.1865-1873

[2]LiebigsAnnalenderChemie,1981,p.1865-1873

59159-39-6

86302-43-4

[1]Patent:US2007/265243,2007,A1.Locationinpatent:Page/Pagecolumn4

[2]Heterocycles,2007,vol.73,p.751-768

[3]ChemischeBerichte,1986,vol.119,p.1196-1207

[4]TetrahedronLetters,1984,vol.25,p.4959-4962

[5]CarbohydrateResearch,1996,vol.281,p.69-77

[6]TetrahedronLetters,2004,vol.45,p.1679-1681

[7]JournalofOrganicChemistry,2001,vol.66,p.4625-4629

[8]Patent:US4855086,1989,A

[9]AdvancedSynthesisandCatalysis,2009,vol.351,p.1423-1430

[10]BioorganicandMedicinalChemistry,2010,vol.18,p.5224-5233

[11]AdvancedSynthesisandCatalysis,2018,vol.360,p.1510-1516

[12]TetrahedronLetters,2019,vol.60,p.1885-1890

[13]OrganicLetters,2019,vol.21,p.7055-7059

Literature

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