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Home Other Building Blocks 6240-11-5
6240-11-5,MFCD00074756
Catalog No.:AA003DU6

6240-11-5 | 1-Adamantaneethanol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$15.00   $11.00
- +
5g
98%
in stock  
$72.00   $50.00
- +
25g
98%
in stock  
$308.00   $216.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003DU6
Chemical Name:
1-Adamantaneethanol
CAS Number:
6240-11-5
Molecular Formula:
C12H20O
Molecular Weight:
180.2866
MDL Number:
MFCD00074756
SMILES:
OCCC12CC3CC(C2)CC(C1)C3
Properties
Properties
 
BP:
275.1°C at 760 mmHg  
Form:
Solid  
MP:
66-69 °C(lit.)  
Refractive Index:
1.5050 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
168  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
3.4  

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,2005,vol.127,p.8720-8731

[2]Patent:JP6196581,2017,B2.Locationinpatent:Paragraph0198

[3]JournalofMedicinalChemistry,1995,vol.38,p.443-452

[4]NewJournalofChemistry,2020,vol.44,p.7071-7079

[5]Journalofmedicinalchemistry,1972,vol.15,p.1313-1321

[6]Patent:US5202321,1993,A

[7]Patent:US5314900,1994,A

[8]Patent:US6335343,2002,B1.Locationinpatent:Pagecolumn65

[9]SyntheticCommunications,2013,vol.43,p.1772-1777

[10]SupramolecularChemistry,2015,vol.27,p.364-371

[11]RussianJournalofOrganicChemistry,2018,vol.54,p.996-1002    Zh.Org.Khim.,2018,vol.54,p.994-1000,7

[1]JournalofHeterocyclicChemistry,1991,vol.28,p.97-108

[1]JournalofMedicinalChemistry,1994,vol.37,p.845-859

[1]JournalofMedicinalChemistry,1988,vol.31,p.1651-1656

[1]Patent:WO2008/73623,2008,A2.Locationinpatent:Page/Pagecolumn95;96

[2]BioorganicandMedicinalChemistry,2011,vol.19,p.3384-3393

[3]ChemicalCommunications,2020,vol.56,p.5969-5972

[4]JournalofOrganicChemistry,1987,vol.52,p.1487-1492

[5]OrganicLetters,2019,vol.21,p.3866-3870

[6]Patent:WO2018/81530,2018,A1.Locationinpatent:Page/Pagecolumn59

[7]OrganicandBiomolecularChemistry,2018,vol.16,p.2541-2548

[8]ChemistryLetters,2017,vol.46,p.580-582

[9]HelveticaChimicaActa,1979,vol.62,p.956-964

[10]JournaloftheAmericanChemicalSociety,2005,vol.127,p.8826-8828

[11]Patent:US2006/189830,2006,A1.Locationinpatent:Page/Pagecolumn8

[12]BioorganicandMedicinalChemistryLetters,2009,vol.19,p.1066-1070

[13]AdvancedSynthesisandCatalysis,2010,vol.352,p.2177-2182

[14]BioorganicandMedicinalChemistryLetters,2011,vol.21,p.5353-5357

[15]BioorganicandMedicinalChemistryLetters,2013,vol.23,p.2532-2537

[16]JournalofMedicinalChemistry,2016,vol.59,p.6826-6837

Literature

Title: Synthesis and photodynamic properties of adamantylethoxy Zn(II) phthalocyanine derivatives in different media and in human red blood cells.

Journal: European journal of medicinal chemistry 20120401

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

Title: Enhancing tumor vaccines: catalyzing MHC class II peptide exchange.

Journal: Expert review of vaccines 20100201

Title: Enhancement of tumour-specific immune responses in vivo by 'MHC loading-enhancer' (MLE).

Journal: PloS one 20090101

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SDS
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