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Home Amines 13989-82-7
13989-82-7,MFCD00019892
Catalog No.:AA007Z0E

13989-82-7 | 4-(Dimethylamino)butyronitrile

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
95%
in stock  
$44.00   $31.00
- +
5g
95%
in stock  
$112.00   $78.00
- +
10g
95%
in stock  
$178.00   $125.00
- +
25g
95%
in stock  
$361.00   $253.00
- +
100g
95%
in stock  
$1,208.00   $846.00
- +
  • 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:
AA007Z0E
Chemical Name:
4-(Dimethylamino)butyronitrile
CAS Number:
13989-82-7
Molecular Formula:
C6H12N2
Molecular Weight:
112.1729
MDL Number:
MFCD00019892
SMILES:
N#CCCCN(C)C
NSC Number:
163159
Properties
Computed Properties
 
Complexity:
87.9  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
3  
XLogP3:
0.3  

Upstream Synthesis Route

[1]Patent:WO2016/41925,2016,A1,.Locationinpatent:Page/Pagecolumn256;257

[1]EuropeanJournalofMedicinalChemistry,2010,vol.45,#1,p.405-410

[2]Patent:US2004/63696,2004,A1,.Locationinpatent:Page/Pagecolumn4

[1]JournalofMedicinalChemistry,2003,vol.46,#6,p.936-953

[2]Hoppe-Seyler'sZeitschriftfuerPhysiologischeChemie,1927,vol.171,p.250

[3]JournaloftheAmericanChemicalSociety,1960,vol.82,p.2386-2389

[4]PharmaceuticalChemistryJournal,1972,vol.6,#1,p.14-17

[5]Khimiko-FarmatsevticheskiiZhurnal,1972,vol.6,#1,p.15-18

[6]Journalofmedicinalchemistry,1963,vol.6,p.275-283

[7]BulletindelaSocieteChimiquedeFrance,1960,p.1162-1165

[1]Patent:US5077288,1991,A,

[1]JournaloftheAmericanChemicalSociety,1945,vol.67,p.1618

Downstream Synthesis Route
3034-52-4    13989-82-7   
4-dimethylamino-2,2-bis-thiazol-2-yl-butyronitrile 

[1]JournaloftheAmericanChemicalSociety,1951,vol.73,p.5752,5756

109-04-6    13989-82-7   
(3,3-di-2pyridyl-propyl)-dimethyl-amine 

[1]JournaloftheAmericanChemicalSociety,1951,vol.73,p.5752,5756

[1]EuropeanJournalofMedicinalChemistry,2010,vol.45,p.405-410

[2]Patent:US5637691,1997,A

[3]Patent:US5721226,1998,A

[4]JournaloftheAmericanChemicalSociety,1945,vol.67,p.1618

[5]Hoppe-Seyler'sZeitschriftfurPhysiologischeChemie,1927,vol.171,p.250

[6]JournaloftheAmericanChemicalSociety,1960,vol.82,p.2386-2389

[7]CollectionofCzechoslovakChemicalCommunications,1977,vol.42,p.1838-1850

[8]JournaloftheAmericanChemicalSociety,1964,vol.86,p.2224-2229

[9]Journalofmedicinalchemistry,1963,vol.6,p.275-283

[10]BulletindelaSocieteChimiquedeFrance,1960,p.1162-1165

[11]JournalofOrganicChemistryUSSR(EnglishTranslation),1968,vol.4,p.122-125    ZhurnalOrganicheskoiKhimii,1968,vol.4,p.128-133

[12]Patent:US2004/63696,2004,A1.Locationinpatent:Page/Pagecolumn4

[13]EuropeanJournalofInorganicChemistry,2011,p.3381-3386

[14]Chemistry-AEuropeanJournal,2014,vol.20,p.4227-4231

[1]Hoppe-Seyler'sZeitschriftfurPhysiologischeChemie,1927,vol.171,p.250

[1]JournalofMedicinalChemistry,2003,vol.46,p.936-953

[2]Hoppe-Seyler'sZeitschriftfurPhysiologischeChemie,1927,vol.171,p.250

[3]JournaloftheAmericanChemicalSociety,1960,vol.82,p.2386-2389

[4]Journalofmedicinalchemistry,1963,vol.6,p.275-283

[5]BulletindelaSocieteChimiquedeFrance,1960,p.1162-1165

Literature
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