1H-BENZ(F)INDENE

C1C=CC2=CC3=C(C=CC=C3)C=C12

InChIKey=LJVOKUMRGBIJGP-UHFFFAOYSA-N

InChI=1S/C13H10/c1-2-5-11-9-13-7-3-6-12(13)8-10(11)4-1/h1-6,8-9H,7H2

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

PubMed

Title	Date	PubMed
Palladium-catalyzed potassium enoxyborate alkylation of enantiopure Hajos-Parrish indenone to construct rearranged steroid ring systems.	2007-06-22	17530900
Neurosteroid analogues. 11. Alternative ring system scaffolds: gamma-aminobutyric acid receptor modulation and anesthetic actions of benz[f]indenes.	2006-07-27	16854065
First synthesis of enantiopure 1,6-difunctionalized dodecahydrobenz[f]indenes.	2005-02-04	15675880
Facile synthetic access to multisubstituted benz[f]indenones and their application as ligands to the first synthesis of group(IV) metallocene complexes.	2003-08-21	12917004
Cyclopentadiene annulated polycyclic aromatic hydrocarbons: investigations of electron affinities.	2003-01-29	12537506

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:14:19 GMT 2025` Edited by `admin` on `Mon Mar 31 19:14:19 GMT 2025`
Record UNII	9J9B82A512
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

1H-BENZ(F)INDENE

Preferred Name

English

Code System Code Type Description

CAS

268-40-6

Created by admin on Mon Mar 31 19:14:19 GMT 2025 , Edited by admin on Mon Mar 31 19:14:19 GMT 2025

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EPA CompTox

DTXSID00181303

Created by admin on Mon Mar 31 19:14:19 GMT 2025 , Edited by admin on Mon Mar 31 19:14:19 GMT 2025

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PUBCHEM

6451436

Created by admin on Mon Mar 31 19:14:19 GMT 2025 , Edited by admin on Mon Mar 31 19:14:19 GMT 2025

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FDA UNII

9J9B82A512

Created by admin on Mon Mar 31 19:14:19 GMT 2025 , Edited by admin on Mon Mar 31 19:14:19 GMT 2025

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