74654-07-2,MFCD17215909
Catalog No.:AA0032ZP

74654-07-2 | 2-(2-(2-Methoxyethoxy)ethoxy)ethanamine

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Purity
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100mg
95%
in stock  
$13.00   $9.00
- +
250mg
95%
in stock  
$16.00   $11.00
- +
1g
98%
in stock  
$22.00   $16.00
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5g
95%
in stock  
$79.00   $55.00
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100g
98%
in stock  
$1,567.00 $1,097.00
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0032ZP
Chemical Name:
2-(2-(2-Methoxyethoxy)ethoxy)ethanamine
CAS Number:
74654-07-2
Molecular Formula:
C7H17NO3
Molecular Weight:
163.2148
MDL Number:
MFCD17215909
SMILES:
COCCOCCOCCN
Properties
Properties
 
BP:
106℃ (11 Torr)  
Form:
Liquid  
Refractive Index:
1.4395 (589.3 nm 20℃)  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
70.7  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
8  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-1.3  

Upstream Synthesis Route

[1]Patent:WO2015/191433,2015,A1,.Locationinpatent:Paragraph0041

[2]ChemischeBerichte,1980,vol.113,#5,p.1691-1707

[3]Molecules,2015,vol.20,#9,p.16085-16102

[4]Chemistry-AnAsianJournal,2011,vol.6,#1,p.149-156

[5]AngewandteChemie-InternationalEdition,2017,vol.56,#48,p.15461-15465

[6]Angew.Chem.,2017,vol.129,p.15664-15669,6

[7]Macromolecules,2012,vol.45,#12,p.5151-5156

[8]Organometallics,2014,vol.33,#16,p.4323-4335

[9]JournalofOrganicChemistry,2018,vol.83,#4,p.1903-1912

[10]Patent:WO2016/40891,2016,A2,.Locationinpatent:Paragraph00304

[11]ChemicalCommunications,2014,vol.50,#54,p.7139-7142

[12]JournaloftheAmericanChemicalSociety,2015,vol.137,#51,p.16196-16202

[13]JournaloftheAmericanChemicalSociety,2012,vol.134,#2,p.844-847

[14]EuropeanJournalofMedicinalChemistry,1991,vol.26,#4,p.461-467

[15]JournaloftheAmericanChemicalSociety,1994,vol.116,#12,p.5057-5062

[16]EuropeanJournalofOrganicChemistry,2001,#10,p.1903-1915

[17]JournalofOrganicChemistry,2011,vol.76,#15,p.6271-6276

[18]ChemicalCommunications,2011,vol.47,#46,p.12491-12493

[19]Macromolecules,2012,vol.45,#3,p.1362-1374

[20]JournaloftheAmericanChemicalSociety,2015,vol.137,#23,p.7286-7289

[21]Patent:WO2015/143185,2015,A1,.Locationinpatent:Paragraph00810

[22]JournalofPolymerScience,PartA:PolymerChemistry,2016,vol.54,#20,p.3294-3302

[23]Patent:US2017/65496,2017,A1,.Locationinpatent:Paragraph0077

[1]Patent:EP2774915,2014,A1,.Locationinpatent:Paragraph0054;0056

[2]EuropeanJournalofOrganicChemistry,2010,#21,p.3991-4003

[3]JournaloftheAmericanChemicalSociety,1994,vol.116,#12,p.5057-5062

[4]JournalofOrganicChemistry,2011,vol.76,#15,p.6271-6276

[5]Chemistry-AnAsianJournal,2011,vol.6,#1,p.149-156

[6]ChemicalCommunications,2011,vol.47,#46,p.12491-12493

[7]JournaloftheAmericanChemicalSociety,2012,vol.134,#2,p.844-847

[8]Macromolecules,2012,vol.45,#12,p.5151-5156

[9]ChemicalCommunications,2014,vol.50,#54,p.7139-7142

[10]JournaloftheAmericanChemicalSociety,2015,vol.137,#23,p.7286-7289

[11]Patent:WO2015/143185,2015,A1,

[12]Molecules,2015,vol.20,#9,p.16085-16102

[13]Patent:WO2016/40891,2016,A2,

[14]Patent:US2017/65496,2017,A1,

[15]JournalofOrganicChemistry,2018,vol.83,#4,p.1903-1912

[1]JournalofMolecularStructure,2011,vol.990,#1-3,p.121-131

[2]BioorganicandMedicinalChemistryLetters,2010,vol.20,#11,p.3280-3283

[3]Synthesis,2002,#6,p.816-824

[4]ChemicalCommunications,2015,vol.51,#32,p.6948-6951

[5]AustralianJournalofChemistry,2015,vol.68,#1,p.57-68

[6]BioorganicandMedicinalChemistry,2007,vol.15,#1,p.186-193

[7]ChemicalCommunications,2013,vol.49,#45,p.5177-5179

[8]Patent:US2016/175292,2016,A1,.Locationinpatent:Sheet4

[1]ChemischeBerichte,1980,vol.113,#5,p.1691-1707

[2]Patent:WO2015/191433,2015,A1,

[3]JournalofPolymerScience,PartA:PolymerChemistry,2016,vol.54,#20,p.3294-3302

[4]JournaloftheAmericanChemicalSociety,2017,vol.139,#17,p.6234-6241

[5]Patent:WO2008/112257,2008,A1,.Locationinpatent:Page/Pagecolumn34-35

[1]BioorganicandMedicinalChemistry,2007,vol.15,#1,p.186-193

[2]Synthesis,2002,#6,p.816-824

[3]EuropeanJournalofOrganicChemistry,2001,#10,p.1903-1915

[4]JournaloftheAmericanChemicalSociety,1994,vol.116,#12,p.5057-5062

[5]ChemischeBerichte,1980,vol.113,#5,p.1691-1707

[6]EuropeanJournalofMedicinalChemistry,1991,vol.26,#4,p.461-467

[7]ChemischeBerichte,1979,vol.112,p.1392-1399

[8]Patent:US6262029,2001,B1,

[9]JournalofMolecularStructure,2011,vol.990,#1-3,p.121-131

[10]JournalofOrganicChemistry,2011,vol.76,#15,p.6271-6276

[11]Chemistry-AnAsianJournal,2011,vol.6,#1,p.149-156

[12]ChemicalCommunications,2011,vol.47,#46,p.12491-12493

[13]JournaloftheAmericanChemicalSociety,2012,vol.134,#2,p.844-847

[14]Macromolecules,2012,vol.45,#12,p.5151-5156

[15]ChemicalCommunications,2013,vol.49,#45,p.5177-5179

[16]ChemicalCommunications,2014,vol.50,#54,p.7139-7142

[17]ChemicalCommunications,2015,vol.51,#32,p.6948-6951

[18]JournaloftheAmericanChemicalSociety,2015,vol.137,#23,p.7286-7289

[19]Patent:WO2015/143185,2015,A1,

[20]Molecules,2015,vol.20,#9,p.16085-16102

[21]Patent:WO2015/191433,2015,A1,

[22]JournaloftheAmericanChemicalSociety,2015,vol.137,#51,p.16196-16202

[23]Patent:WO2016/40891,2016,A2,

[24]JournalofPolymerScience,PartA:PolymerChemistry,2016,vol.54,#20,p.3294-3302

[25]Patent:US2017/65496,2017,A1,

[26]JournaloftheAmericanChemicalSociety,2017,vol.139,#17,p.6234-6241

[27]AngewandteChemie-InternationalEdition,2017,vol.56,#48,p.15461-15465

[28]Angew.Chem.,2017,vol.129,p.15664-15669,6

[29]JournalofOrganicChemistry,2018,vol.83,#4,p.1903-1912

[30]JournalofOrganicChemistry,2018,vol.83,#4,p.1903-1912

[31]Patent:WO2008/112257,2008,A1,

Downstream Synthesis Route

[1]Schmidt,Manfred;Amstutz,Rene;Crass,Gerhard;Seebach,Dieter[ChemischeBerichte,1980,vol.113,#5,p.1691-1707]

[1]CurrentPatentAssignee:NEKTARTHERAPEUTICS-US2005/136031,2005,A1Locationinpatent:Page/Pagecolumn19

[1]Chemistry-AEuropeanJournal,2011,vol.17,p.1818-1827

[1]Szigethy,Geza;Raymond,KennethN.[Chemistry-AEuropeanJournal,2011,vol.17,#6,p.1818-1827]

53003-10-4    74654-07-2   
CASUnavailable 

[1]Locationinpatent:experimentalpartHuczynski,Adam;Janczak,Jan;Stefanska,Joanna;Antoszczak,Michal;Brzezinski,Bogumil[BioorganicandMedicinalChemistryLetters,2012,vol.22,#14,p.4697-4702]

Literature

Title: Schiff base of gossypol with 3,6,9-trioxa-decylamine complexes with monovalent cations studied by mass spectrometry, (1)H-NMR, FTIR, and PM5 semiempirical methods.

Journal: Biopolymers 20040301

Title: Nianhe Han, et al. The derivant of aplysiatoxin 10 and application thereof. CN106279352A.

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SDS
Tags:74654-07-2 Molecular Formula|74654-07-2 MDL|74654-07-2 SMILES|74654-07-2 2-(2-(2-Methoxyethoxy)ethoxy)ethanamine
Catalog No.: AA0032ZP
74654-07-2,MFCD17215909
74654-07-2 | 2-(2-(2-Methoxyethoxy)ethoxy)ethanamine
Pack Size: 100mg
Purity: 95%
in stock
$13.00 $9.00
Pack Size: 250mg
Purity: 95%
in stock
$16.00 $11.00
Pack Size: 1g
Purity: 98%
in stock
$22.00 $16.00
Pack Size: 5g
Purity: 95%
in stock
$79.00 $55.00
Pack Size: 100g
Purity: 98%
in stock
$1,567.00 $1,097.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0032ZP
Chemical Name: 2-(2-(2-Methoxyethoxy)ethoxy)ethanamine
CAS Number: 74654-07-2
Molecular Formula: C7H17NO3
Molecular Weight: 163.2148
MDL Number: MFCD17215909
SMILES: COCCOCCOCCN
Properties
BP: 106℃ (11 Torr)  
Form: Liquid  
Refractive Index: 1.4395 (589.3 nm 20℃)  
Storage: Keep in dry area;2-8℃;  
Complexity: 70.7  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 8  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -1.3  
Upstream Synthesis Route
74654-06-1    74654-07-2 

[1]Patent:WO2015/191433,2015,A1,.Locationinpatent:Paragraph0041

[2]ChemischeBerichte,1980,vol.113,#5,p.1691-1707

[3]Molecules,2015,vol.20,#9,p.16085-16102

[4]Chemistry-AnAsianJournal,2011,vol.6,#1,p.149-156

[5]AngewandteChemie-InternationalEdition,2017,vol.56,#48,p.15461-15465

[6]Angew.Chem.,2017,vol.129,p.15664-15669,6

[7]Macromolecules,2012,vol.45,#12,p.5151-5156

[8]Organometallics,2014,vol.33,#16,p.4323-4335

[9]JournalofOrganicChemistry,2018,vol.83,#4,p.1903-1912

[10]Patent:WO2016/40891,2016,A2,.Locationinpatent:Paragraph00304

[11]ChemicalCommunications,2014,vol.50,#54,p.7139-7142

[12]JournaloftheAmericanChemicalSociety,2015,vol.137,#51,p.16196-16202

[13]JournaloftheAmericanChemicalSociety,2012,vol.134,#2,p.844-847

[14]EuropeanJournalofMedicinalChemistry,1991,vol.26,#4,p.461-467

[15]JournaloftheAmericanChemicalSociety,1994,vol.116,#12,p.5057-5062

[16]EuropeanJournalofOrganicChemistry,2001,#10,p.1903-1915

[17]JournalofOrganicChemistry,2011,vol.76,#15,p.6271-6276

[18]ChemicalCommunications,2011,vol.47,#46,p.12491-12493

[19]Macromolecules,2012,vol.45,#3,p.1362-1374

[20]JournaloftheAmericanChemicalSociety,2015,vol.137,#23,p.7286-7289

[21]Patent:WO2015/143185,2015,A1,.Locationinpatent:Paragraph00810

[22]JournalofPolymerScience,PartA:PolymerChemistry,2016,vol.54,#20,p.3294-3302

[23]Patent:US2017/65496,2017,A1,.Locationinpatent:Paragraph0077

62921-74-8    74654-07-2 

[1]Patent:EP2774915,2014,A1,.Locationinpatent:Paragraph0054;0056

[2]EuropeanJournalofOrganicChemistry,2010,#21,p.3991-4003

[3]JournaloftheAmericanChemicalSociety,1994,vol.116,#12,p.5057-5062

[4]JournalofOrganicChemistry,2011,vol.76,#15,p.6271-6276

[5]Chemistry-AnAsianJournal,2011,vol.6,#1,p.149-156

[6]ChemicalCommunications,2011,vol.47,#46,p.12491-12493

[7]JournaloftheAmericanChemicalSociety,2012,vol.134,#2,p.844-847

[8]Macromolecules,2012,vol.45,#12,p.5151-5156

[9]ChemicalCommunications,2014,vol.50,#54,p.7139-7142

[10]JournaloftheAmericanChemicalSociety,2015,vol.137,#23,p.7286-7289

[11]Patent:WO2015/143185,2015,A1,

[12]Molecules,2015,vol.20,#9,p.16085-16102

[13]Patent:WO2016/40891,2016,A2,

[14]Patent:US2017/65496,2017,A1,

[15]JournalofOrganicChemistry,2018,vol.83,#4,p.1903-1912

167221-50-3    74654-07-2 

[1]JournalofMolecularStructure,2011,vol.990,#1-3,p.121-131

[2]BioorganicandMedicinalChemistryLetters,2010,vol.20,#11,p.3280-3283

[3]Synthesis,2002,#6,p.816-824

[4]ChemicalCommunications,2015,vol.51,#32,p.6948-6951

[5]AustralianJournalofChemistry,2015,vol.68,#1,p.57-68

[6]BioorganicandMedicinalChemistry,2007,vol.15,#1,p.186-193

[7]ChemicalCommunications,2013,vol.49,#45,p.5177-5179

[8]Patent:US2016/175292,2016,A1,.Locationinpatent:Sheet4

74654-05-0    74654-07-2 

[1]ChemischeBerichte,1980,vol.113,#5,p.1691-1707

[2]Patent:WO2015/191433,2015,A1,

[3]JournalofPolymerScience,PartA:PolymerChemistry,2016,vol.54,#20,p.3294-3302

[4]JournaloftheAmericanChemicalSociety,2017,vol.139,#17,p.6234-6241

[5]Patent:WO2008/112257,2008,A1,.Locationinpatent:Page/Pagecolumn34-35

112-35-6    74654-07-2 

[1]BioorganicandMedicinalChemistry,2007,vol.15,#1,p.186-193

[2]Synthesis,2002,#6,p.816-824

[3]EuropeanJournalofOrganicChemistry,2001,#10,p.1903-1915

[4]JournaloftheAmericanChemicalSociety,1994,vol.116,#12,p.5057-5062

[5]ChemischeBerichte,1980,vol.113,#5,p.1691-1707

[6]EuropeanJournalofMedicinalChemistry,1991,vol.26,#4,p.461-467

[7]ChemischeBerichte,1979,vol.112,p.1392-1399

[8]Patent:US6262029,2001,B1,

[9]JournalofMolecularStructure,2011,vol.990,#1-3,p.121-131

[10]JournalofOrganicChemistry,2011,vol.76,#15,p.6271-6276

[11]Chemistry-AnAsianJournal,2011,vol.6,#1,p.149-156

[12]ChemicalCommunications,2011,vol.47,#46,p.12491-12493

[13]JournaloftheAmericanChemicalSociety,2012,vol.134,#2,p.844-847

[14]Macromolecules,2012,vol.45,#12,p.5151-5156

[15]ChemicalCommunications,2013,vol.49,#45,p.5177-5179

[16]ChemicalCommunications,2014,vol.50,#54,p.7139-7142

[17]ChemicalCommunications,2015,vol.51,#32,p.6948-6951

[18]JournaloftheAmericanChemicalSociety,2015,vol.137,#23,p.7286-7289

[19]Patent:WO2015/143185,2015,A1,

[20]Molecules,2015,vol.20,#9,p.16085-16102

[21]Patent:WO2015/191433,2015,A1,

[22]JournaloftheAmericanChemicalSociety,2015,vol.137,#51,p.16196-16202

[23]Patent:WO2016/40891,2016,A2,

[24]JournalofPolymerScience,PartA:PolymerChemistry,2016,vol.54,#20,p.3294-3302

[25]Patent:US2017/65496,2017,A1,

[26]JournaloftheAmericanChemicalSociety,2017,vol.139,#17,p.6234-6241

[27]AngewandteChemie-InternationalEdition,2017,vol.56,#48,p.15461-15465

[28]Angew.Chem.,2017,vol.129,p.15664-15669,6

[29]JournalofOrganicChemistry,2018,vol.83,#4,p.1903-1912

[30]JournalofOrganicChemistry,2018,vol.83,#4,p.1903-1912

[31]Patent:WO2008/112257,2008,A1,

Downstream Synthesis Route
74654-07-2    51952-13-7 

[1]Schmidt,Manfred;Amstutz,Rene;Crass,Gerhard;Seebach,Dieter[ChemischeBerichte,1980,vol.113,#5,p.1691-1707]

4759-48-2    74654-07-2    854601-58-4 

[1]CurrentPatentAssignee:NEKTARTHERAPEUTICS-US2005/136031,2005,A1Locationinpatent:Page/Pagecolumn19

2483-46-7    74654-07-2    1278583-70-2 

[1]Chemistry-AEuropeanJournal,2011,vol.17,p.1818-1827

74654-07-2    104010-92-6    1278583-67-7 

[1]Szigethy,Geza;Raymond,KennethN.[Chemistry-AEuropeanJournal,2011,vol.17,#6,p.1818-1827]

53003-10-4    74654-07-2   
CASUnavailable 

[1]Locationinpatent:experimentalpartHuczynski,Adam;Janczak,Jan;Stefanska,Joanna;Antoszczak,Michal;Brzezinski,Bogumil[BioorganicandMedicinalChemistryLetters,2012,vol.22,#14,p.4697-4702]

Literature fold

Title: Schiff base of gossypol with 3,6,9-trioxa-decylamine complexes with monovalent cations studied by mass spectrometry, (1)H-NMR, FTIR, and PM5 semiempirical methods.

Journal: Biopolymers20040301

Title: Nianhe Han, et al. The derivant of aplysiatoxin 10 and application thereof. CN106279352A.

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