Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H18N3P |
| Molecular Weight | 163.201 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(C)P(N(C)C)N(C)C
InChI
InChIKey=XVDBWWRIXBMVJV-UHFFFAOYSA-N
InChI=1S/C6H18N3P/c1-7(2)10(8(3)4)9(5)6/h1-6H3
| Molecular Formula | C6H18N3P |
| Molecular Weight | 163.201 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Fullerene derivatives incorporating phosphoramidous ylide and phosphoramidate: synthesis and property. | 2009-07-03 |
|
| Synthesis and characterization of the trihalophosphine compounds of ruthenium [RuX2(eta(6)-cymene)(PY3)] (X = Cl, Br, Y = F, Cl, Br) and the related PF2(NMe2) and P(NMe2)3 compounds; multinuclear NMR spectroscopy and the X-ray single crystal structures of [RuBr2(eta(6)-cymene)(PF3)], [RuBr2(eta(6)-cymene)(PF2{NMe2})], and [RuI2(eta(6)-cymene)(P{NMe2}3)]. | 2008-10-20 |
|
| Synthesis of bulky arylphosphanes by rhodium-catalyzed formal [2+2+2] cycloaddition reaction and their use as ligands. | 2008-09-01 |
|
| BINOL-derived phosphoramidites in asymmetric hydrogenation: can the presence of a functionality in the amino group influence the catalytic outcome? | 2008-04 |
|
| Sugar derived hexacoordinated phosphates: chiral anionic auxiliaries with general asymmetric efficiency. | 2008-03 |
|
| BINOL-3,3'-triflone N,N-dimethyl phosphoramidites: through-space 19F,31P spin-spin coupling with a remarkable dependency on temperature and solvent internal pressure. | 2008 |
|
| Synthesis of transient and stable C-amino phosphorus ylides and their fragmentation into transient and stable carbenes. | 2006-01-18 |
|
| Phosphorus-based p-tert-butylcalix[5]arene ligands. | 2004-05-03 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:12:33 GMT 2025
by
admin
on
Mon Mar 31 19:12:33 GMT 2025
|
| Record UNII |
6072HG2UW4
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
Tris(dimethylamino)phosphine
Created by
admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
|
PRIMARY | |||
|
1608-26-0
Created by
admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
|
PRIMARY | |||
|
DTXSID6061816
Created by
admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
|
PRIMARY | |||
|
6072HG2UW4
Created by
admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
|
PRIMARY | |||
|
300000053392
Created by
admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
|
PRIMARY | |||
|
216-534-4
Created by
admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
|
PRIMARY | |||
|
102707
Created by
admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
|
PRIMARY | |||
|
15355
Created by
admin on Mon Mar 31 19:12:33 GMT 2025 , Edited by admin on Mon Mar 31 19:12:33 GMT 2025
|
PRIMARY |