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Home Amines 31037-02-2
31037-02-2,MFCD00003294
Catalog No.:AA0031VT

31037-02-2 | Ethyl 5-amino-1-methylpyrazole-4-carboxylate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
97%
in stock  
$6.00   $4.00
- +
10g
97%
in stock  
$7.00   $5.00
- +
25g
97%
in stock  
$9.00   $7.00
- +
100g
97%
in stock  
$26.00   $18.00
- +
  • 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:
AA0031VT
Chemical Name:
Ethyl 5-amino-1-methylpyrazole-4-carboxylate
CAS Number:
31037-02-2
Molecular Formula:
C7H11N3O2
Molecular Weight:
169.1811
MDL Number:
MFCD00003294
SMILES:
CCOC(=O)c1cnn(c1N)C
Properties
Properties
 
BP:
300.5°C at 760 mmHg  
Form:
Solid  
MP:
101-102 °C  
Stability:
Hygroscopic  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
174  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
0.7  

Upstream Synthesis Route

[1]JournalofMedicinalChemistry,2018,vol.61,#19,p.8670-8692

[2]BioorganicandMedicinalChemistryLetters,2004,vol.14,#17,p.4585-4589

[3]JournalofHeterocyclicChemistry,2007,vol.44,#4,p.749-755

[4]Patent:EP1512687,2005,A1,.Locationinpatent:Page/Pagecolumn6

[5]Patent:US5498630,1996,A,

[6]PakistanJournalofScientificandIndustrialResearch,2005,vol.48,#5,p.318-321

[1]JournalofOrganicChemistry,2016,vol.81,#11,p.4883-4889

[2]JournalofHeterocyclicChemistry,2014,vol.51,#SUPPL.1,p.E216-E221

[3]Patent:US4620865,1986,A,

[4]Patent:WO2008/52974,2008,A1,.Locationinpatent:Page/Pagecolumn42

[5]BioorganicandMedicinalChemistry,2009,vol.17,#9,p.3379-3387

[6]Patent:WO2007/62805,2007,A1,.Locationinpatent:Page/Pagecolumn68

[1]JournalofHeterocyclicChemistry,2001,vol.38,#5,p.1045-1050

[2]Patent:US5849779,1998,A,

[3]HelveticaChimicaActa,1959,vol.42,p.349,358

[1]EuropeanJournalofMedicinalChemistry,2017,vol.136,p.330-333

[1]OrganicLetters,2015,vol.17,#12,p.2964-2967

[2]OrganicLetters,2015,vol.17,#12,p.2964-2967

Downstream Synthesis Route

[1]JournalofHeterocyclicChemistry,2001,vol.38,p.1045-1050

[2]Patent:US5849779,1998,A

[3]HelveticaChimicaActa,1959,vol.42,p.349,358

[1]LiebigsAnnalenderChemie,1985,p.1910-1916

[2]Heterocycles,1988,vol.27,p.105-112

[3]RSCAdvances,2014,vol.4,p.1782-1793

[1]JournalofMedicinalChemistry,2018,vol.61,p.8670-8692

[2]BioorganicandMedicinalChemistryLetters,2004,vol.14,p.4585-4589

[3]Patent:EP1512687,2005,A1.Locationinpatent:Page/Pagecolumn6

[4]JournalofMedicinalChemistry,1989,vol.32,p.2573-2582

[1]Wamhoff,Heinrich;Haffmanns,Guenter[ChemischeBerichte,1984,vol.117,#2,p.585-621]

[2]Taylor;Patel[JournalofHeterocyclicChemistry,1992,vol.28,#8,p.1857-1861]

[1]LiebigsAnnalenderChemie,1985,p.1910-1916

[2]JournalofHeterocyclicChemistry,2007,vol.44,p.749-755

[3]LiebigsAnnalenderChemie,1985,p.1910-1916

Literature

Title: 2-aminothienopyridazines as novel adenosine A1 receptor allosteric modulators and antagonists.

Journal: Journal of medicinal chemistry 20081009

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SDS
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