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22009-37-6,MFCD00087600
Catalog No.:AA003NDM

22009-37-6 | 7-Methyl-1-tetralone

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$6.00   $4.00
- +
1g
98%
in stock  
$12.00   $8.00
- +
5g
98%
in stock  
$36.00   $25.00
- +
10g
98%
in stock  
$55.00   $39.00
- +
25g
98%
in stock  
$92.00   $64.00
- +
100g
98%
in stock  
$365.00   $256.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003NDM
Chemical Name:
7-Methyl-1-tetralone
CAS Number:
22009-37-6
Molecular Formula:
C11H12O
Molecular Weight:
160.2124
MDL Number:
MFCD00087600
SMILES:
Cc1ccc2c(c1)C(=O)CCC2
NSC Number:
115847
Properties
Properties
 
BP:
287.1±25.0°C at 760 mmHg  
Form:
Solid  
MP:
35-38°C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
185  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
1  
XLogP3:
2.4  

Upstream Synthesis Route

[1]TetrahedronLetters,2003,vol.44,#21,p.4007-4010

[2]ChemistryLetters,2008,vol.37,#3,p.320-321

[3]AustralianJournalofChemistry,1990,vol.43,p.1547-1557

[4]AdvancedSynthesisandCatalysis,2018,vol.360,#15,p.2894-2899

[5]ChemischeBerichte,1923,vol.56,p.630

[6]ChemischeBerichte,1923,vol.56,p.1431

[7]JournaloftheChemicalSociety,1954,p.798

[8]JournaloftheChemicalSociety,1933,p.434,436

[9]BulletindelaSocieteChimiquedeFrance,1970,p.146-150

[10]JournaloftheAmericanChemicalSociety,1974,vol.96,#16,p.5130-5138

[11]JournaloftheChemicalSociety,1961,p.4794-4808

[12]JournalofOrganicChemistry,1962,vol.27,p.857-863

[13]JournalofMedicinalChemistry,1977,vol.20,#8,p.1059-1064

[14]JournalofHeterocyclicChemistry,1989,vol.26,p.1305-1318

[15]HelveticaChimicaActa,1932,vol.15,p.907,914

[16]Arkivoc,2010,vol.2010,#9,p.40-53

[17]JournalofMolecularStructure,2010,vol.980,#1-3,p.59-65

[1]HelveticaChimicaActa,1932,vol.15,p.907,914

[2]JournaloftheAmericanChemicalSociety,1936,vol.58,p.572,575

[3]HelveticaChimicaActa,1936,vol.19,p.377,383

[4]JournaloftheAmericanChemicalSociety,1953,vol.75,p.347

[5]BulletindelaSocieteChimiquedeFrance,1958,p.1448,1457

[6]JournaloftheChemicalSociety,1956,p.3857,3860

[7]JournalofMedicinalChemistry,2008,vol.51,#23,p.7625-7634

[1]SyntheticCommunications,1993,vol.23,#19,p.2701-2708

[1]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2003,vol.42,#3,p.593-601

[1]Journalofmedicinalchemistry,1970,vol.13,#1,p.87-89

[2]AustralianJournalofChemistry,1990,vol.43,p.1547-1557

[3]JournalofOrganicChemistry,1962,vol.27,p.857-863

[4]AdvancedSynthesisandCatalysis,2018,vol.360,#15,p.2894-2899

Downstream Synthesis Route

[1]JournalofOrganicChemistry,1949,vol.14,p.492,496

[1]AustralianJournalofChemistry,1990,vol.43,p.1547-1557

[2]BulletindelaSocieteChimiquedeFrance,1958,p.1448,1457

[3]BulletindelaSocieteChimiquedeFrance,1956,p.1631,1633

[4]AustralianJournalofChemistry,1975,vol.28,p.2669-2680

[5]JournaloftheChemicalSociety,1961,p.4794-4808

[1]TetrahedronLetters,2003,vol.44,p.4007-4010

[2]ChemistryLetters,2008,vol.37,p.320-321

[3]AustralianJournalofChemistry,1990,vol.43,p.1547-1557

[4]AdvancedSynthesisandCatalysis,2018,vol.360,p.2894-2899

[5]ChemischeBerichte,1923,vol.56,p.630

[6]ChemischeBerichte,1923,vol.56,p.1431

[7]JournaloftheChemicalSociety,1954,p.798

[8]JournaloftheChemicalSociety,1933,p.434,436

[9]BulletindelaSocieteChimiquedeFrance,1970,p.146-150

[10]JournaloftheAmericanChemicalSociety,1974,vol.96,p.5130-5138

[11]JournalofOrganicChemistry,1962,vol.27,p.857-863

[12]JournalofMedicinalChemistry,1977,vol.20,p.1059-1064

[13]HelveticaChimicaActa,1932,vol.15,p.907,914

[14]ARKIVOC,2010,vol.2010,p.40-53

[15]JournalofMolecularStructure,2010,vol.980,p.59-65

[16]JournalofHeterocyclicChemistry,2019,vol.56,p.1672-1683

[1]TetrahedronLetters,1981,vol.22,p.603-606

[1]JournalofOrganicChemistry,1974,vol.39,p.1416-1420

Literature
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