Catalog No.:AA003G4A

24300-91-2 | 2,7-Di-tert-butylpyrene

Name: Name:2,7-Di-tert-butylpyrene
Brand: AABLOCKS
SKU: AA003G4A
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in stock

$15.00 $10.00

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97%

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$66.00 $46.00

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10g

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$128.00 $89.00

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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA003G4A

Chemical Name:

2,7-Di-tert-butylpyrene

CAS Number:

24300-91-2

Molecular Formula:

C24H26

Molecular Weight:

314.4632

MDL Number:

MFCD01013641

SMILES:

CC(c1cc2ccc3c4c2c(c1)ccc4cc(c3)C(C)(C)C)(C)C

Properties

BP:

448°C at 760 mmHg

Form:

Solid

MP:

207.0 to 211.0 °C

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

389

Covalently-Bonded Unit Count:

Heavy Atom Count:

Rotatable Bond Count:

XLogP3:

8.4

Downstream Synthesis Route

129-00-0

507-20-0

24300-91-2

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[2]Patent:US2008/119671,2008,A1.Locationinpatent:Page/Pagecolumn14-15

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[4]Patent:CN105601636,2016,A.Locationinpatent:Paragraph0022;0023

[5]AngewandteChemie-InternationalEdition,2017,vol.56,p.13031-13035 Angew.Chem.,2017,vol.129,p.13211-13215,5

[6]JournalofMaterialsChemistryC,2016,vol.4,p.3809-3814

[7]ChineseChemicalLetters,2011,vol.22,p.819-822

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[16]ChemicalCommunications,2011,vol.47,p.514-516

[17]Molecules,2011,vol.16,p.4467-4481

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[20]RSCAdvances,2019,vol.9,p.19641-19647

[21]Patent:CN109942585,2019,A.Locationinpatent:Paragraph0098;0101-0104

129-00-0

507-20-0

24300-91-2

78751-62-9

[1]RecueildesTravauxChimiquesdesPays-Bas,1988,vol.107,p.529-535

[2]JournalofOrganicChemistry,1994,vol.59,p.3294-3300

[3]Chemistry-AEuropeanJournal,2013,vol.19,p.16295-16302

[4]JournalofOrganicChemistry,1994,vol.59,p.3294-3300

24300-91-2

129-00-0

[1]JournalofOrganicChemistry,1991,vol.56,p.1334-1337

24300-91-2

69080-03-1

69618-59-3

69618-61-7

69618-58-2

[1]ActachemicaScandinavica.SeriesB:Organicchemistryandbiochemistry,1986,vol.40,p.665-677

24300-91-2

76466-34-7

[1]Patent:CN105601636,2016,A.Locationinpatent:Paragraph0024;0025

[2]AngewandteChemie-InternationalEdition,2017,vol.56,p.13031-13035 Angew.Chem.,2017,vol.129,p.13211-13215,5

[3]JournaloftheChemicalSociety.PerkintransactionsI,1997,p.1201-1207

[4]EuropeanJournalofOrganicChemistry,2010,p.72-79

[5]OrganicandBiomolecularChemistry,2012,vol.10,p.2255-2262

[6]Patent:US2008/119671,2008,A1.Locationinpatent:Page/Pagecolumn15

[7]JournalofOrganicChemistry,1995,vol.60,p.1070-1073

[8]ChineseChemicalLetters,2011,vol.22,p.819-822

[9]JournaloftheAmericanChemicalSociety,1982,vol.104,p.3701-3707

[10]JournalofOrganicChemistry,2009,vol.74,p.7544-7547

[11]ChemistryLetters,1980,p.1127-1130

[12]JournaloftheChemicalSociety.PerkinTransactions2(2001),1996,vol.3,p.359-364

[13]JournaloftheChemicalSociety.PerkintransactionsI,1997,p.1201-1207

[14]Molecules,2011,vol.16,p.4467-4481

Literature

Title: General method for the synthesis of crystalline organic nanorods using porous alumina templates.

Journal: Chemical communications (Cambridge, England) 20060321

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SDS