Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C7H12O |
| Molecular Weight | 112.1696 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1CCCCC1=O
InChI
InChIKey=LFSAPCRASZRSKS-UHFFFAOYSA-N
InChI=1S/C7H12O/c1-6-4-2-3-5-7(6)8/h6H,2-5H2,1H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| The Suzuki coupling reaction in the stereocontrolled synthesis of 9-cis-retinoic acid and its ring-demethylated analogues. | 2001 Dec 14 |
|
| Catalytic Meerwein-Pondorf-Verley reduction by simple aluminum complexes. | 2001 Jul 26 |
|
| Lithium hexamethyldisilazide/triethylamine-mediated ketone enolization: remarkable rate accelerations stemming from a dimer-based mechanism. | 2003 Apr 9 |
|
| Unfunctionalized, alpha-epimerizable nonracemic ketones and aldehydes can be accessed by crystallization-induced dynamic resolution of imines. | 2003 Mar 19 |
|
| Lithium hexamethyldisilazide-mediated ketone enolization: the influence of hindered dialkyl ethers and isostructural dialkylamines on reaction rates and mechanisms. | 2004 Jan 23 |
|
| Reaction of ketones with lithium hexamethyldisilazide: competitive enolizations and 1,2-additions. | 2004 Mar 17 |
|
| High stereoselectivity on low temperature Diels-Alder reactions. | 2005 Dec 9 |
|
| Enolate structure and electron affinity. | 2005 Oct 6 |
|
| N-(2,6-Dimethyl-3-oxo-1-thia-4-aza-spiro-[4.5]dec-4-yl)-2-hydr-oxy-2,2-di-phenyl-acetamide. | 2008 Sep 13 |
|
| 1-Methyl-2,4-bis-(2-methoxy-phen-yl)-3-aza-bicyclo-[3.3.1]nonan-9-one. | 2009 Nov 18 |
|
| New 3H-indole synthesis by Fischer's method. Part I. | 2010 Apr 8 |
|
| 2,4-Bis(4-chloro-phen-yl)-1-methyl-3-aza-bicyclo-[3.3.1]nonan-9-one. | 2010 Feb 6 |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
JECFA EVALUATION |
2-METHYLCYCLOHEXANONE
Created by
admin on Fri Dec 15 21:16:00 GMT 2023 , Edited by admin on Fri Dec 15 21:16:00 GMT 2023
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
56E8224ZFJ
Created by
admin on Fri Dec 15 21:16:00 GMT 2023 , Edited by admin on Fri Dec 15 21:16:00 GMT 2023
|
PRIMARY | |||
|
1034
Created by
admin on Fri Dec 15 21:16:00 GMT 2023 , Edited by admin on Fri Dec 15 21:16:00 GMT 2023
|
PRIMARY | |||
|
DTXSID6052245
Created by
admin on Fri Dec 15 21:16:00 GMT 2023 , Edited by admin on Fri Dec 15 21:16:00 GMT 2023
|
PRIMARY | |||
|
209-513-6
Created by
admin on Fri Dec 15 21:16:00 GMT 2023 , Edited by admin on Fri Dec 15 21:16:00 GMT 2023
|
PRIMARY | |||
|
524
Created by
admin on Fri Dec 15 21:16:00 GMT 2023 , Edited by admin on Fri Dec 15 21:16:00 GMT 2023
|
PRIMARY | |||
|
C532535
Created by
admin on Fri Dec 15 21:16:00 GMT 2023 , Edited by admin on Fri Dec 15 21:16:00 GMT 2023
|
PRIMARY | |||
|
11419
Created by
admin on Fri Dec 15 21:16:00 GMT 2023 , Edited by admin on Fri Dec 15 21:16:00 GMT 2023
|
PRIMARY | |||
|
583-60-8
Created by
admin on Fri Dec 15 21:16:00 GMT 2023 , Edited by admin on Fri Dec 15 21:16:00 GMT 2023
|
PRIMARY | |||
|
2917
Created by
admin on Fri Dec 15 21:16:00 GMT 2023 , Edited by admin on Fri Dec 15 21:16:00 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD
