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3680-71-5,MFCD08445809
Catalog No.:AA0035H9

3680-71-5 | Pyrrolo[2,3-d]pyrimidin-4-ol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$6.00   $4.00
- +
5g
98%
in stock  
$7.00   $5.00
- +
10g
98%
in stock  
$11.00   $8.00
- +
25g
98%
in stock  
$17.00   $12.00
- +
100g
98%
in stock  
$66.00   $47.00
- +
500g
98%
in stock  
$328.00   $230.00
- +
  • 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:
AA0035H9
Chemical Name:
Pyrrolo[2,3-d]pyrimidin-4-ol
CAS Number:
3680-71-5
Molecular Formula:
C6H5N3O
Molecular Weight:
135.1234
MDL Number:
MFCD08445809
SMILES:
O=c1nc[nH]c2c1cc[nH]2
Properties
Properties
 
BP:
473°C at 760 mmHg  
Form:
Solid  
MP:
239.894 °C  
Solubility:
Soluble in dimethyl sulfoxide.  
Stability:
Moisture & Light Sensitive  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
189  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
XLogP3:
-0.2  

Upstream Synthesis Route

[1]BioorganicandMedicinalChemistryLetters,2004,vol.14,#21,p.5247-5250

[2]LiebigsAnnalenderChemie,1983,#9,p.1576-1587

[1]Patent:US5753664,1998,A,

[1]BioorganicandMedicinalChemistryLetters,2010,vol.20,#24,p.7297-7298

[2]BioorganicandMedicinalChemistryLetters,2004,vol.14,#21,p.5247-5250

[3]EuropeanJournalofMedicinalChemistry,2008,vol.43,#6,p.1248-1260

[1]RussianJournalofBioorganicChemistry,1995,vol.21,#11,p.756-761

[2]BioorganicheskayaKhimiya,1995,vol.21,#11,p.874-880

[3]Patent:US2002/183319,2002,A1,

[1]BioorganicandMedicinalChemistryLetters,2004,vol.14,#21,p.5247-5250

[2]EuropeanJournalofOrganicChemistry,1998,#5,p.827-835

[3]RussianJournalofBioorganicChemistry,1995,vol.21,#11,p.756-761

[4]BioorganicheskayaKhimiya,1995,vol.21,#11,p.874-880

Downstream Synthesis Route

[1]LiebigsAnnalenderChemie,1982,vol.No.4,p.805-812

[1]BioorganicandMedicinalChemistryLetters,2004,vol.14,p.5247-5250

[2]EuropeanJournalofOrganicChemistry,1998,p.827-835

[3]RussianJournalofBioorganicChemistry,1995,vol.21,p.756-761    BioorganicheskayaKhimiya,1995,vol.21,p.874-880

[1]Patent:US5235053,1993,A

[1]Patent:CN107827893,2018,A.Locationinpatent:Paragraph00500058;0064;0066;0067;0068

[2]Patent:US2010/160356,2010,A1.Locationinpatent:Page/Pagecolumn33

[3]Patent:CN105622616,2016,A.Locationinpatent:Paragraph0053;0054;0055

[4]Patent:CN108794479,2018,A.Locationinpatent:Paragraph0008;0020

[5]Patent:US2010/190981,2010,A1.Locationinpatent:Page/Pagecolumn100-101

[6]BioorganicandMedicinalChemistry,2012,vol.20,p.6770-6789

[7]Patent:WO2007/104944,2007,A1.Locationinpatent:Page/Pagecolumn44

[8]CanadianJournalofChemistry,2018,vol.96,p.1093-1100

[9]Patent:WO2010/14930,2010,A2.Locationinpatent:Page/Pagecolumn61

[10]Patent:WO2006/46023,2006,A1.Locationinpatent:Page/Pagecolumn123-124

[11]Patent:WO2008/75109,2008,A1.Locationinpatent:Page/Pagecolumn113

[12]Patent:WO2006/46024,2006,A1.Locationinpatent:Page/Pagecolumn118

[13]Patent:WO2007/125321,2007,A2.Locationinpatent:Page/Pagecolumn117

[14]Patent:WO2007/125315,2007,A2.Locationinpatent:Page/Pagecolumn122

[15]EuropeanJournalofPharmaceuticalSciences,2014,vol.59,p.69-82

[16]Patent:WO2018/29641,2018,A1.Locationinpatent:Page/Pagecolumn7

[17]ArchivderPharmazie,2018,vol.351

[1]Patent:WO2010/14930,2010,A2.Locationinpatent:Page/Pagecolumn60-61

[2]Patent:US2010/160356,2010,A1.Locationinpatent:Page/Pagecolumn33

[3]Patent:WO2007/104944,2007,A1

[4]Patent:WO2007/125315,2007,A2

Literature

Title: Studies on the glycosylation of pyrrolo[2,3-d] pyrimidines with 1-O-acetyl-2,3,5-tri-O-benzoyl-beta-D-ribofuranose: the formation of regioisomers during toyocamycin and 7-deazainosine syntheses.

Journal: Nucleosides, nucleotides & nucleic acids 20090501

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