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17061-62-0,MFCD00277836
Catalog No.:AA003587

17061-62-0 | Bis-(4-methoxybenzyl)amine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
≥98%
in stock  
$11.00   $8.00
- +
25g
98%
in stock  
$43.00   $30.00
- +
100g
98%
in stock  
$115.00   $80.00
- +
500g
98%
in stock  
$424.00 $297.00
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003587
Chemical Name:
Bis-(4-methoxybenzyl)amine
CAS Number:
17061-62-0
Molecular Formula:
C16H19NO2
Molecular Weight:
257.3276
MDL Number:
MFCD00277836
SMILES:
COc1ccc(cc1)CNCc1ccc(cc1)OC
Properties
Properties
 
BP:
384°C at 760 mmHg  
Form:
Solid  
MP:
35-37℃  
Storage:
Room Temperature;Light sensitive;Inert atmosphere;  

Computed Properties
 
Complexity:
207  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
19  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
6  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
2.7  

Literature

Title: Electronic coupling between two amine redox sites through the 5,5'-positions of metal-chelating 2,2'-bipyridines.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20121105

Title: Highly twisted triarylamines for photoinduced intramolecular charge transfer.

Journal: The journal of physical chemistry. A 20110804

Title: Electronic communication between two amine redox centers bridged by a bis(terpyridine)ruthenium(II) complex.

Journal: Inorganic chemistry 20110801

Title: A new special pair model comprising meso-di-p-anisylaminoporphyrin: enhancement of visible-light absorptivities and quantification of electronic communication in mixed-valent cation radical.

Journal: Chemical communications (Cambridge, England) 20100328

Title: Highly substituted azulene dyes as multifunctional NLO and electron-transfer compounds.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20030905

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SDS
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Tags:17061-62-0 Molecular Formula|17061-62-0 MDL|17061-62-0 SMILES|17061-62-0 Bis-(4-methoxybenzyl)amine
Catalog No.: AA003587
17061-62-0,MFCD00277836
17061-62-0 | Bis-(4-methoxybenzyl)amine
Pack Size： 5g
Purity： ≥98%
in stock
$11.00 $8.00
Pack Size： 25g
Purity： 98%
in stock
$43.00 $30.00
Pack Size： 100g
Purity： 98%
in stock
$115.00 $80.00
Pack Size： 500g
Purity： 98%
in stock
$424.00 $297.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003587
Chemical Name: Bis-(4-methoxybenzyl)amine
CAS Number: 17061-62-0
Molecular Formula: C16H19NO2
Molecular Weight: 257.3276
MDL Number: MFCD00277836
SMILES: COc1ccc(cc1)CNCc1ccc(cc1)OC
Properties
BP: 384°C at 760 mmHg  
Form: Solid  
MP: 35-37℃  
Storage: Room Temperature;Light sensitive;Inert atmosphere;  
Complexity: 207  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 19  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 6  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 2.7  
Literature fold

Title: Electronic coupling between two amine redox sites through the 5,5'-positions of metal-chelating 2,2'-bipyridines.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20121105

Title: Highly twisted triarylamines for photoinduced intramolecular charge transfer.

Journal: The journal of physical chemistry. A20110804

Title: Electronic communication between two amine redox centers bridged by a bis(terpyridine)ruthenium(II) complex.

Journal: Inorganic chemistry20110801

Title: A new special pair model comprising meso-di-p-anisylaminoporphyrin: enhancement of visible-light absorptivities and quantification of electronic communication in mixed-valent cation radical.

Journal: Chemical communications (Cambridge, England)20100328

Title: Highly substituted azulene dyes as multifunctional NLO and electron-transfer compounds.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20030905

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