1,5-DIAZABICYCLO(4.3.0)NON-5-ENE

C1CN2CCCN=C2C1

InChIKey=SGUVLZREKBPKCE-UHFFFAOYSA-N

InChI=1S/C7H12N2/c1-3-7-8-4-2-6-9(7)5-1/h1-6H2

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

PubMed

Title	Date	PubMed
Friedel-Crafts acylation of pyrroles and indoles using 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) as a nucleophilic catalyst.	2010-12-17	21077631
Formation of zwitterionic fullerodendron using a new DBN-focal dendron.	2010	22315557
Electrospray ionization mass spectrometric analysis of chemical reactions of dissolution of selenium in strongly basic amines.	2005-01	15584008
Natural abundance nitrogen-15 nuclear magnetic resonance spectral studies on selected donors.	2002-10	12396056
P(CH(3)NCH(2)CH(2))(3)N as a dehydrobromination reagent: synthesis of vitamin A derivatives revisited.	2002-01-25	11798312

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:19:29 GMT 2025` Edited by `admin` on `Mon Mar 31 21:19:29 GMT 2025`
Record UNII	978M4OL12Q
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

1,5-DIAZABICYCLO(4.3.0)NON-5-ENE

Systematic Name

English

NSC-118106

Preferred Name

English

NBU

Common Name

English

1,5-DIAZABICYCLO(4.3.0)NON-5-ENE [MI]

Common Name

English

DBN

Common Name

English

2,3,4,6,7,8-HEXAHYDROPYRROLO(1,2-A)PYRIMIDINE

Systematic Name

English

Code System Code Type Description

CAS

3001-72-7