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7287-81-2,MFCD00046635
Catalog No.:AA00FIIZ

7287-81-2 | 1-(m-Tolyl)ethanol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
97%
in stock  
$14.00   $10.00
- +
250mg
97%
in stock  
$24.00   $17.00
- +
1g
97
in stock  
$86.00   $60.00
- +
5g
97
in stock  
$229.00   $160.00
- +
25g
97
in stock  
$722.00   $505.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00FIIZ
Chemical Name:
1-(m-Tolyl)ethanol
CAS Number:
7287-81-2
Molecular Formula:
C9H12O
Molecular Weight:
136.1910
MDL Number:
MFCD00046635
SMILES:
Cc1cccc(c1)C(O)C
Properties
Computed Properties
 
Complexity:
101  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
1  
XLogP3:
1.8  

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1958,vol.80,p.3076,3079

[1]Patent:WO2013/120104,2013,A2.Locationinpatent:Paragraph00340

[2]Patent:WO2017/37116,2017,A1.Locationinpatent:Page/Pagecolumn71

[3]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,1984,vol.23,p.60-62

[4]ChemischeBerichte,1922,vol.55,p.42

[5]AngewandteChemie-InternationalEdition,2019,vol.58,p.10330-10334    Angew.Chem.,2019,vol.131,p.10437-10442,6

[1]TetrahedronLetters,2014,vol.55,p.1585-1588

[2]Chemistry-AEuropeanJournal,2012,vol.18,p.11550-11554

[3]ChemicalScience,2019,vol.10,p.4883-4889

[4]BulletinoftheChemicalSocietyofJapan,1989,vol.62,p.4069-4071

[5]BeilsteinJournalofOrganicChemistry,2017,vol.13,p.2049-2055

[6]Organometallics,2018,vol.37,p.584-591

[7]Synlett,2018,vol.29,p.447-451

[8]JournalofOrganicChemistry,1997,vol.62,p.4916-4920

[9]ChemCatChem,2017,vol.9,p.1113-1118

[10]Patent:CN106588957,2017,A.Locationinpatent:Paragraph0033

[11]Molecules,2019,vol.24

[12]BulletinoftheChemicalSocietyofJapan,1990,vol.63,p.2433-2434

[13]GreenChemistry,2016,vol.18,p.4605-4610

[14]AdvancedSynthesisandCatalysis,2018,vol.360,p.4293-4300

[15]AppliedOrganometallicChemistry,2016,vol.30,p.645-652

[16]ACSCatalysis,2014,vol.4,p.3994-4003

[17]ACSCatalysis,2017,vol.7,p.7226-7230

[18]ChemistryLetters,2017,vol.46,p.808-810

[19]OrganicLetters,2007,vol.9,p.109-111

[20]ACSCatalysis,2014,vol.4,p.2889-2895

[21]ChemicalandPharmaceuticalBulletin,2017,vol.65,p.801-804

[22]JustusLiebigsAnnalenderChemie,1915,vol.408,p.244    ChemischeBerichte,1916,vol.49,p.2400

[23]JournaloftheChemicalSociety,1957,p.5087

[24]RussianJournalofGeneralChemistry,2014,vol.84,p.2016-2020    Zh.Obshch.Khim.,2014,vol.84,p.2016-2020,5

[25]JournalofOrganicChemistry,2015,vol.80,p.10769-10776

[26]Organometallics,2017,vol.36,p.3638-3644

[27]ChemicalScience,2017,vol.8,p.7476-7482

[28]InorganicChemistry,2017,vol.56,p.11282-11298

[29]Organometallics,2018,vol.37,p.603-617

[30]Organometallics,2018,vol.37,p.2732-2740

[31]EuropeanJournalofMedicinalChemistry,2018,vol.159,p.90-103

[32]InorganicChemistry,2019,vol.58,p.4945-4953

[33]CanadianJournalofChemistry,1965,vol.43,p.479

[1]JustusLiebigsAnnalenderChemie,1915,vol.408,p.244    ChemischeBerichte,1916,vol.49,p.2400

Literature
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SDS
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