Details
Stereochemistry | ACHIRAL |
Molecular Formula | C7H12N2 |
Molecular Weight | 124.1836 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C1CN2CCCN=C2C1
InChI
InChIKey=SGUVLZREKBPKCE-UHFFFAOYSA-N
InChI=1S/C7H12N2/c1-3-7-8-4-2-6-9(7)5-1/h1-6H2
Molecular Formula | C7H12N2 |
Molecular Weight | 124.1836 |
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 |
---|---|---|
P(CH(3)NCH(2)CH(2))(3)N as a dehydrobromination reagent: synthesis of vitamin A derivatives revisited. | 2002 Jan 25 |
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Natural abundance nitrogen-15 nuclear magnetic resonance spectral studies on selected donors. | 2002 Oct |
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Electrospray ionization mass spectrometric analysis of chemical reactions of dissolution of selenium in strongly basic amines. | 2005 Jan |
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Formation of zwitterionic fullerodendron using a new DBN-focal dendron. | 2010 |
|
Friedel-Crafts acylation of pyrroles and indoles using 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) as a nucleophilic catalyst. | 2010 Dec 17 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 03:46:27 GMT 2023
by
admin
on
Sat Dec 16 03:46:27 GMT 2023
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Record UNII |
978M4OL12Q
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Record Status |
Validated (UNII)
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Record Version |
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76349
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978M4OL12Q
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1,5-Diazabicyclo(4.3.0)non-5-ene
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m4265
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DTXSID10184087
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118106
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221-087-3
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