+1 858-523-8231
Login | Register
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
Home Aldehydes 33016-47-6
33016-47-6,MFCD07409972
Catalog No.:AA0032RD

33016-47-6 | 1-Trityl-1H-imidazole-4-carboxaldehyde

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$10.00   $7.00
- +
5g
98%
in stock  
$13.00   $9.00
- +
10g
98%
in stock  
$16.00   $11.00
- +
25g
97%
in stock  
$34.00   $24.00
- +
100g
97%
in stock  
$133.00   $93.00
- +
  • 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:
AA0032RD
Chemical Name:
1-Trityl-1H-imidazole-4-carboxaldehyde
CAS Number:
33016-47-6
Molecular Formula:
C23H18N2O
Molecular Weight:
338.4018
MDL Number:
MFCD07409972
SMILES:
O=Cc1ncn(c1)C(c1ccccc1)(c1ccccc1)c1ccccc1
Properties
Properties
 
BP:
502.8°C at 760 mmHg  
Form:
Solid  
MP:
180-190°C  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
402  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
26  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
5  
XLogP3:
4.6  

Upstream Synthesis Route

[1]JournalofHeterocyclicChemistry,1985,vol.22,p.57-59

[2]JournalofHeterocyclicChemistry,1985,vol.22,p.57-59

[1]JournalofHeterocyclicChemistry,1985,vol.22,p.57-59

[2]Tetrahedron,1992,vol.48,#21,p.4327-4346

[1]BioorganicandMedicinalChemistry,2009,vol.17,#23,p.7993-8002

[2]Patent:WO2008/4096,2008,A1,.Locationinpatent:Page/Pagecolumn79

[3]JournalofMedicinalChemistry,2002,vol.45,#1,p.177-188

[4]EuropeanJournalofOrganicChemistry,2015,vol.2015,#18,p.3957-3962

[5]Patent:US2004/122018,2004,A1,.Locationinpatent:Page317

[6]OrganicandBiomolecularChemistry,2011,vol.9,#7,p.2274-2278

[7]JournalofMedicinalChemistry,2011,vol.54,#6,p.1693-1703

[8]AngewandteChemie-InternationalEdition,2005,vol.44,#31,p.4903-4906

[9]JournalofMedicinalChemistry,2006,vol.49,#19,p.5710-5727

[10]Patent:WO2006/102159,2006,A2,.Locationinpatent:Page/Pagecolumn21;22

[11]Chemistry-AEuropeanJournal,2006,vol.12,#16,p.4321-4332

[12]Synlett,2016,vol.27,#19,p.2734-2736

[13]ChemicalCommunications,2011,vol.47,#48,p.12855-12857

[14]Patent:US6143766,2000,A,

[15]JournalofMedicinalChemistry,2010,vol.53,#4,p.1712-1725

[16]Patent:WO2008/94992,2008,A2,.Locationinpatent:Page/Pagecolumn188

[17]TetrahedronLetters,2006,vol.47,#8,p.1253-1255

[18]Patent:WO2012/173280,2012,A1,.Locationinpatent:Page/Pagecolumn35-36

[19]Patent:US2003/199522,2003,A1,

[20]Patent:US2002/82272,2002,A1,

[21]Patent:WO2010/52256,2010,A1,.Locationinpatent:Page/Pagecolumn37

[22]Patent:WO2010/52255,2010,A1,.Locationinpatent:Page/Pagecolumn68

[23]Patent:WO2006/23720,2006,A2,.Locationinpatent:Page/Pagecolumn48

[24]Patent:US2007/49616,2007,A1,.Locationinpatent:Page/Pagecolumn29

[25]Patent:EP2848618,2015,A1,.Locationinpatent:Paragraph0816

[26]ChemMedChem,2018,vol.13,#8,p.842-851

[1]Patent:US2003/229099,2003,A1,.Locationinpatent:Page269

[2]JournalofMedicinalChemistry,2010,vol.53,#10,p.3887-3898

[3]BioorganicandMedicinalChemistryLetters,2013,vol.23,#23,p.6492-6499

[4]OrganicProcessResearchandDevelopment,2000,vol.4,#6,p.613-614

[5]JournalofMedicinalChemistry,2007,vol.50,#19,p.4585-4605

[6]JournalofMedicinalChemistry,2009,vol.52,#12,p.3703-3715

[1]BioorganicandMedicinalChemistry,1997,vol.5,#10,p.1989-1998

[2]JournalofHeterocyclicChemistry,1991,vol.28,#8,p.1941-1944

[3]J.Med.Chem.,1996,vol.39,#2,p.353-358

[4]Patent:EP1382607,2004,A2,.Locationinpatent:Page28

[5]SyntheticCommunications,1987,vol.17,#2,p.223-228

[6]Tetrahedron,2000,vol.56,#13,p.1837-1850

[7]CollectionofCzechoslovakChemicalCommunications,2002,vol.67,#9,p.1335-1344

[8]JournalofOrganicChemistry,2002,vol.67,#3,p.620-624

[9]Patent:US2002/193596,2002,A1,

[10]Patent:US5034539,1991,A,

Downstream Synthesis Route
96797-15-8    68-12-2    15469-97-3   
4-iodo-2-formyl-1-tritylimidazole 
  67478-50-6    33016-47-6 

[1]JournalofHeterocyclicChemistry,1985,vol.22,p.57-59

[2]JournalofHeterocyclicChemistry,1985,vol.22,p.57-59

[1]JournalofMedicinalChemistry,1990,vol.33,p.317-327

[1]BulletindelaSocieteChimiquedeFrance,1994,vol.131,p.590-599

[2]BulletindelaSocieteChimiquedeFrance,1994,vol.131,p.590-599

diethyl(cyanomethyl)phosphonate 
  33016-47-6    154312-79-5 

[1]Adger,BrianM.;Surtees,John[SyntheticCommunications,1987,vol.17,#2,p.223-228]

[1]Filipiak,T.;Seliga,C.;Frankowski,A.[PolishJournalofChemistry,1995,vol.69,#2,p.259-263]

Literature
Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Related Products of 33016-47-6
191103-80-7

191103-80-7

 82594-80-7

82594-80-7

 116795-55-2

116795-55-2

 464924-63-8

464924-63-8

 76074-88-9

76074-88-9

 85102-93-8

85102-93-8
Building Blocks
More >
Tags:33016-47-6 Molecular Formula|33016-47-6 MDL|33016-47-6 SMILES|33016-47-6 1-Trityl-1H-imidazole-4-carboxaldehyde |Organic_Building_Blocks