Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H12O3 |
| Molecular Weight | 192.2112 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC2=C(C=C1OC)C(=O)CC2
InChI
InChIKey=IHMQOBPGHZFGLC-UHFFFAOYSA-N
InChI=1S/C11H12O3/c1-13-10-5-7-3-4-9(12)8(7)6-11(10)14-2/h5-6H,3-4H2,1-2H3
5,6-Dimethoxy-1-Indanone is used for the organic synthesis. It is an intermediate useful in the preparation of acetylcholinesterase inhibitor Donepezil. 5,6-Dimethoxy-1-Indanone derivatives displayed a potent suppression of the hepatitis C virus (HCV) replication and inhibition of bovine viral diarrhea virus RNA synthesis.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Dopamine D(3) receptor antagonists. 1. Synthesis and structure-activity relationships of 5,6-dimethoxy-N-alkyl- and N-alkylaryl-substituted 2-aminoindans. | 2001 Dec 20 |
|
| Synthesis of novel, potentially biologically active dibenzosuberone derivatives. | 2005 Dec 31 |
|
| Simple and regioselective bromination of 5,6-disubstituted-indan-1-ones with Br2 under acidic and basic conditions. | 2007 Jan 29 |
|
| Photochemical synthesis of substituted indan-1-ones related to donepezil. | 2008 May |
|
| Methyl 5,6-dimeth-oxy-1H-indole-2-carboxyl-ate. | 2009 Sep 5 |
|
| (2E)-2-Benzyl-idene-5,6-dimethoxy-indan-1-one. | 2010 Sep 11 |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
F805RZI8GO
Created by
admin on Sat Dec 16 08:49:33 GMT 2023 , Edited by admin on Sat Dec 16 08:49:33 GMT 2023
|
PRIMARY | |||
|
DTXSID9057680
Created by
admin on Sat Dec 16 08:49:33 GMT 2023 , Edited by admin on Sat Dec 16 08:49:33 GMT 2023
|
PRIMARY | |||
|
401450
Created by
admin on Sat Dec 16 08:49:33 GMT 2023 , Edited by admin on Sat Dec 16 08:49:33 GMT 2023
|
PRIMARY | |||
|
75018
Created by
admin on Sat Dec 16 08:49:33 GMT 2023 , Edited by admin on Sat Dec 16 08:49:33 GMT 2023
|
PRIMARY | |||
|
2107-69-9
Created by
admin on Sat Dec 16 08:49:33 GMT 2023 , Edited by admin on Sat Dec 16 08:49:33 GMT 2023
|
PRIMARY | |||
|
218-287-8
Created by
admin on Sat Dec 16 08:49:33 GMT 2023 , Edited by admin on Sat Dec 16 08:49:33 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD
