Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H18N2 |
| Molecular Weight | 130.2312 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(C)CCCN(C)C
InChI
InChIKey=DMQSHEKGGUOYJS-UHFFFAOYSA-N
InChI=1S/C7H18N2/c1-8(2)6-5-7-9(3)4/h5-7H2,1-4H3
| Molecular Formula | C7H18N2 |
| Molecular Weight | 130.2312 |
| 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 |
|---|---|---|
| Copper/alpha-ketocarboxylate chemistry with supporting peralkylated diamines: reactivity of copper(I) complexes and dicopper-oxygen intermediates. | 2010-04-05 |
|
| (2,2'-Biquinoline-κN,N')dichlorido-iron(II). | 2009-10-17 |
|
| Ionothermal synthesis, crystal structure and solid-state NMR spectroscopy of a new organically templated gallium oxalatophosphate: (H2TMPD)0.5[Ga3(C2O4)0.5(PO4)3] (TMPD=N,N,N',N'-tetramethyl-1,3-propanediamine). | 2007-10-28 |
|
| Solvation in electrospray mass spectrometry: effects on the reaction kinetics of fragmentation mediated by ion-neutral complexes. | 2005-06-24 |
|
| Spectral, electrochemical and molecular orbital studies on solvatochromic mixed ligand copper(II) complexes of malonate and diamine derivatives. | 2003-04 |
|
| Consequences of correlated solvation on the structures and reactivities of RLi-diamine complexes: 1,2-addition and alpha-lithiation reactions of imines by TMEDA-solvated n-butyllithium and phenyllithium. | 2002-01-16 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:04:46 GMT 2025
by
admin
on
Mon Mar 31 22:04:46 GMT 2025
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| Record UNII |
73B9I6HN5R
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| Record Status |
Validated (UNII)
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| Record Version |
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203-818-8
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8084
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110-95-2
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