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768-49-0,MFCD00008899
Catalog No.:AA003HIT

768-49-0 | (2-Methylprop-1-en-1-yl)benzene

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100mg
97%
in stock  
$8.00   $6.00
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250mg
97%
in stock  
$16.00   $11.00
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1g
97%
in stock  
$19.00   $14.00
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5g
97%
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$74.00   $52.00
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10g
97%
in stock  
$126.00   $89.00
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25g
97%
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$315.00   $220.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003HIT
Chemical Name:
(2-Methylprop-1-en-1-yl)benzene
CAS Number:
768-49-0
Molecular Formula:
C10H12
Molecular Weight:
132.2023
MDL Number:
MFCD00008899
SMILES:
CC(=Cc1ccccc1)C
NSC Number:
163349
Properties
Properties
 
BP:
187-188°C(lit.)  
Form:
Liquid  
MP:
-50--48°C(lit.)  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
112  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Rotatable Bond Count:
1  
XLogP3:
3.8  

Downstream Synthesis Route

[1]TetrahedronLetters,2006,vol.47,p.8463-8466

[2]CuihuaXuebao/ChineseJournalofCatalysis,2016,vol.37,p.979-986

[3]ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1935,vol.201,p.833    BulletindelaSocieteChimiquedeFrance,1935,vol.<5>2,p.633,636,637

[4]ZhurnalObshcheiKhimii,1949,vol.19,p.1927,1939    Chem.Abstr.,1950,p.1955

[5]ChemischesZentralblatt,1901,vol.72,p.624

[6]JournaloftheChemicalSociety,1925,vol.127,p.94

[7]JournalofOrganicChemistry,1938,vol.3,p.62,72

[8]OrientalJournalofChemistry,2012,vol.28,p.1141-1145

[1]CanadianJournalofChemistry,1989,vol.67,p.689-698

[2]JournalofOrganicChemistry,1996,vol.61,p.324-328

[3]JournaloftheAmericanChemicalSociety,1928,vol.50,p.554

[4]HelveticaChimicaActa,1982,vol.65,p.2061-2070

[5]ChemSusChem,2010,vol.3,p.695-697

[6]InorganicaChimicaActa,2019,vol.489,p.224-229

[1]Patent:US2006/161011,2006,A1.Locationinpatent:Page/Pagecolumn5

[2]OrganicSyntheses,1997,vol.74,p.91-91

[3]AngewandteChemie-InternationalEdition,2014,vol.53,p.4359-4363    Angew.Chem.,2014,vol.126,p.4448-4452,5

[4]JournaloftheAmericanChemicalSociety,2011,vol.133,p.4710-4713

[5]TetrahedronLetters,1984,vol.25,p.2691-2694

[6]JournaloftheAmericanChemicalSociety,2005,vol.127,p.13672-13679

[7]Catalysisscienceandtechnology,2013,vol.3,p.706-714

[8]ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1906,vol.143,p.649    AnnalesdeChimie(Cachan,France),1907,vol.<8>10,p.354

[9]BulletindelaSocieteChimiquedeFrance,1926,vol.<4>39,p.776

[10]JournaloftheAmericanChemicalSociety,1981,vol.103,p.6455-6460

[11]JournaloftheChemicalSociety.PerkintransactionsI,1993,p.1345-1358

[12]BulletinoftheChemicalSocietyofJapan,1984,vol.57,p.2681-2682

[13]JournaloftheChemicalSociety.Chemicalcommunications,1982,p.1352-1353

[14]JournaloftheAmericanChemicalSociety,1995,vol.117,p.9243-9250

[15]OrganicLetters,2005,vol.7,p.987-990

[16]TetrahedronAsymmetry,2006,vol.17,p.372-376

[17]JournalofOrganometallicChemistry,2006,vol.691,p.4419-4433

[18]JournalofMolecularStructure,1983,vol.99,p.259-266

[19]ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1921,vol.172,p.388    BulletindelaSocieteChimiquedeFrance,1921,vol.<4>29,p.817,819

[20]EuropeanJournalofOrganicChemistry,2008,p.4867-4870

[21]InorganicaChimicaActa,2013,vol.406,p.301-306

[22]ChemCatChem,2019,vol.11,p.4907-4915

[1]JournaloftheAmericanChemicalSociety,2001,vol.123,p.9220-9221

[2]Tetrahedron,2010,vol.66,p.8536-8543

[3]AdvancedSynthesisandCatalysis,2006,vol.348,p.1734-1742

[4]TetrahedronLetters,2011,vol.52,p.3137-3140

[5]TetrahedronLetters,2010,vol.51,p.808-810

[6]Synlett,2013,vol.24,p.947-950

[7]ChemicalandPharmaceuticalBulletin,2012,vol.60,p.1594-1598

[8]OrganicLetters,2003,vol.5,p.185-187

[9]TetrahedronLetters,2008,vol.49,p.1071-1075

[10]JournaloftheAmericanChemicalSociety,2001,vol.123,p.1365-1371

[11]CanadianJournalofChemistry,1955,vol.33,p.1002,1025

[12]JournaloftheAmericanChemicalSociety,1999,vol.121,p.11229-11230

[13]Chemistry-AEuropeanJournal,2016,vol.22,p.17552-17556

[14]JournaloftheAmericanChemicalSociety,2017,vol.139,p.5149-5155

[1]ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1922,vol.174,p.1212

Literature

Title: Facile η5-η3 hapticity interconversion in pentamethylcyclopentadienyl ruthenium(II) complexes containing a phenylmethallyl ('open indenyl') ligand.

Journal: Dalton transactions (Cambridge, England : 2003) 20111121

Title: Use of urine volatile organic compounds to discriminate tuberculosis patients from healthy subjects.

Journal: Analytical chemistry 20110715

Title: Bay leaves improve glucose and lipid profile of people with type 2 diabetes.

Journal: Journal of clinical biochemistry and nutrition 20090101

Title: Gas chromatography/mass spectrometry analysis of Laurus nobilis essential oil composition of northern Cyprus.

Journal: Journal of medicinal food 20071201

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