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129940-50-7,MFCD00273373
Catalog No.:AA000TQN

129940-50-7 | (S)-(-)-Trityl glycidyl ether

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
97%
in stock  
$18.00   $13.00
- +
25g
97%
in stock  
$34.00   $24.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA000TQN
Chemical Name:
(S)-(-)-Trityl glycidyl ether
CAS Number:
129940-50-7
Molecular Formula:
C22H20O2
Molecular Weight:
316.3930
MDL Number:
MFCD00273373
SMILES:
O1C[C@H]1COC(c1ccccc1)(c1ccccc1)c1ccccc1
Properties
Properties
 
BP:
438.8°C at 760 mmHg  
Form:
Solid  
MP:
99-102 °C(lit.)  
Refractive Index:
-11 ° (C=1, CHCl3)  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
330  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
24  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
6  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
4.4  

Upstream Synthesis Route

[1]Synthesis,2007,#24,p.3807-3814

[2]TetrahedronLetters,2000,vol.41,#33,p.6323-6326

[3]JournalofOrganicChemistry,2003,vol.68,#8,p.3026-3042

[4]JournalofOrganicChemistry,2013,vol.78,#11,p.5172-5183

[5]Patent:WO2010/53572,2010,A2,.Locationinpatent:Page/Pagecolumn163

[6]ACSChemicalNeuroscience,2018,

[7]TetrahedronLetters,1994,vol.35,#20,p.3243-3246

[8]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1994,#16,p.2229-2236

[9]JournalofOrganicChemistry,1998,vol.63,#6,p.1961-1973

[10]TetrahedronLetters,1999,vol.40,#12,p.2371-2374

[11]Patent:WO2006/14429,2006,A2,.Locationinpatent:Page/Pagecolumn11;figure3

[1]Patent:US6448422,2002,B1,

[1]JournaloftheAmericanChemicalSociety,2012,vol.134,#19,p.8058-8061

[1]BulletinoftheChemicalSocietyofJapan,2007,vol.80,#7,p.1391-1401

[1]JournalofOrganicChemistry,1998,vol.63,#6,p.1961-1973

Downstream Synthesis Route

[1]CollectionofCzechoslovakChemicalCommunications,2000,vol.65,p.1126-1144

[1]CollectionofCzechoslovakChemicalCommunications,2001,vol.66,p.1545-1592

[1]Bioorganicandmedicinalchemistry,2002,vol.10,p.1743-1759

[1]CollectionofCzechoslovakChemicalCommunications,2005,vol.70,p.1465-1481

129940-50-7    70277-75-7   
(S)-1-Trityloxy-pent-4-yn-2-ol 

[1]Tetrahedron,2006,vol.62,p.7687-7698

Literature

Title: Antiviral activity of triazine analogues of 1-(S)-[3-hydroxy-2-(phosphonomethoxy)propyl]cytosine (cidofovir) and related compounds.

Journal: Journal of medicinal chemistry 20070308

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Tags:129940-50-7 Molecular Formula|129940-50-7 MDL|129940-50-7 SMILES|129940-50-7 (S)-(-)-Trityl glycidyl ether
Catalog No.: AA000TQN
129940-50-7,MFCD00273373
129940-50-7 | (S)-(-)-Trityl glycidyl ether
Pack Size： 5g
Purity： 97%
in stock
$18.00 $13.00
Pack Size： 25g
Purity： 97%
in stock
$34.00 $24.00
Quantity
- +
Add to Card
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Technical Information
Catalog Number: AA000TQN
Chemical Name: (S)-(-)-Trityl glycidyl ether
CAS Number: 129940-50-7
Molecular Formula: C22H20O2
Molecular Weight: 316.3930
MDL Number: MFCD00273373
SMILES: O1C[C@H]1COC(c1ccccc1)(c1ccccc1)c1ccccc1
Properties
BP: 438.8°C at 760 mmHg  
Form: Solid  
MP: 99-102 °C(lit.)  
Refractive Index: -11 ° (C=1, CHCl3)  
Storage: Inert atmosphere;2-8℃;  
Complexity: 330  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 24  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 6  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 4.4  
Upstream Synthesis Route
76-83-5    57044-25-4    129940-50-7 

[1]Synthesis,2007,#24,p.3807-3814

[2]TetrahedronLetters,2000,vol.41,#33,p.6323-6326

[3]JournalofOrganicChemistry,2003,vol.68,#8,p.3026-3042

[4]JournalofOrganicChemistry,2013,vol.78,#11,p.5172-5183

[5]Patent:WO2010/53572,2010,A2,.Locationinpatent:Page/Pagecolumn163

[6]ACSChemicalNeuroscience,2018,

[7]TetrahedronLetters,1994,vol.35,#20,p.3243-3246

[8]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1994,#16,p.2229-2236

[9]JournalofOrganicChemistry,1998,vol.63,#6,p.1961-1973

[10]TetrahedronLetters,1999,vol.40,#12,p.2371-2374

[11]Patent:WO2006/14429,2006,A2,.Locationinpatent:Page/Pagecolumn11;figure3

76-83-5    60456-23-7    129940-50-7 

[1]Patent:US6448422,2002,B1,

65291-30-7    16975-62-5    129940-50-7 

[1]JournaloftheAmericanChemicalSociety,2012,vol.134,#19,p.8058-8061

65291-30-7    124-38-9    17327-06-9    22147-30-4    65291-30-7    129940-50-7 

[1]BulletinoftheChemicalSocietyofJapan,2007,vol.80,#7,p.1391-1401

203250-06-0    129940-50-7 

[1]JournalofOrganicChemistry,1998,vol.63,#6,p.1961-1973

Downstream Synthesis Route
6974-78-3    129940-50-7    204771-46-0    303014-69-9 

[1]CollectionofCzechoslovakChemicalCommunications,2000,vol.65,p.1126-1144

120503-69-7    129940-50-7    402575-67-1 

[1]CollectionofCzechoslovakChemicalCommunications,2001,vol.66,p.1545-1592

1515-89-5    129940-50-7    253350-30-0 

[1]Bioorganicandmedicinalchemistry,2002,vol.10,p.1743-1759

25902-89-0    129940-50-7    913274-62-1 

[1]CollectionofCzechoslovakChemicalCommunications,2005,vol.70,p.1465-1481

129940-50-7    70277-75-7   
(S)-1-Trityloxy-pent-4-yn-2-ol 

[1]Tetrahedron,2006,vol.62,p.7687-7698

Literature fold

Title: Antiviral activity of triazine analogues of 1-(S)-[3-hydroxy-2-(phosphonomethoxy)propyl]cytosine (cidofovir) and related compounds.

Journal: Journal of medicinal chemistry20070308

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