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2973-50-4,MFCD00091082
Catalog No.:AA002Z67

2973-50-4 | 2-Aminophenylacetonitrile

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Purity
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Price(USD)
Quantity
  
250mg
97%
in stock  
$36.00   $25.00
- +
1g
97%
in stock  
$44.00   $31.00
- +
5g
97%
in stock  
$162.00   $113.00
- +
10g
97%
in stock  
$295.00   $206.00
- +
25g
97%
in stock  
$602.00   $421.00
- +
100g
97%
in stock  
$2,140.00   $1,498.00
- +
  • 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:
AA002Z67
Chemical Name:
2-Aminophenylacetonitrile
CAS Number:
2973-50-4
Molecular Formula:
C8H8N2
Molecular Weight:
132.1625
MDL Number:
MFCD00091082
SMILES:
N#CCc1ccccc1N
Properties
Properties
 
BP:
302.2°C at 760 mmHg  
Form:
Solid  
MP:
69-72 °C  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
145  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
0.9  

Upstream Synthesis Route

[1]ChemischeBerichte,1884,vol.17,p.506

[2]ChemischeBerichte,1889,vol.22,p.2139

[3]Patent:US2004/9983,2004,A1,.Locationinpatent:Page/Pagecolumn118

[1]AustralianJournalofChemistry,2013,vol.66,#6,p.635-645

[1]ChemicalandPharmaceuticalBulletin,1983,vol.31,#10,p.3424-3445

[1]ChemicalandPharmaceuticalBulletin,1983,vol.31,#10,p.3424-3445

[2]Patent:US2011/111046,2011,A1,.Locationinpatent:Page/Pagecolumn17

[3]Patent:WO2011/58473,2011,A1,.Locationinpatent:Page/Pagecolumn34;35

[4]TetrahedronLetters,2006,vol.47,#2,p.159-162

[5]JournaloftheAmericanChemicalSociety,1950,vol.72,p.3047,3049

[6]HelveticaChimicaActa,1925,vol.8,p.834

[7]ChemischeBerichte,1910,vol.43,p.2550

[8]ChemischeBerichte,1884,vol.17,p.506

[9]ChemischeBerichte,1889,vol.22,p.2139

[10]JournalofMedicinalChemistry,1996,vol.39,#6,p.1201-1209

[11]JournalofMedicinalChemistry,2003,vol.46,#9,p.1661-1669

[12]Patent:EP1367058,2003,A1,.Locationinpatent:Page25-26

[1]JournalofMedicinalChemistry,2003,vol.46,#9,p.1661-1669

Downstream Synthesis Route

[1]ChemischeBerichte,1910,vol.43,p.2550

[1]ChemischeBerichte,1910,vol.43,p.2550

[1]ChemicalandPharmaceuticalBulletin,1983,vol.31,p.3424-3445

[2]Patent:US2011/111046,2011,A1.Locationinpatent:Page/Pagecolumn17

[3]Patent:WO2011/58473,2011,A1.Locationinpatent:Page/Pagecolumn34;35

[4]TetrahedronLetters,2006,vol.47,p.159-162

[5]JournaloftheAmericanChemicalSociety,1950,vol.72,p.3047,3049

[6]HelveticaChimicaActa,1925,vol.8,p.834

[7]ChemischeBerichte,1910,vol.43,p.2550

[8]JournalofMedicinalChemistry,1996,vol.39,p.1201-1209

[9]JournalofMedicinalChemistry,2003,vol.46,p.1661-1669

[10]Patent:EP1367058,2003,A1.Locationinpatent:Page25-26

[1]ChemischeBerichte,1884,vol.17,p.506    ChemischeBerichte,1889,vol.22,p.2139

[2]Patent:US2004/9983,2004,A1.Locationinpatent:Page/Pagecolumn118

[1]JournalofOrganicChemistry,1984,vol.49,p.269-276

[2]Patent:WO2016/102633,2016,A1.Locationinpatent:Page/Pagecolumn71-72

Literature
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SDS
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