Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H14 |
| Molecular Weight | 98.1861 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C1CCCCCC1
InChI
InChIKey=DMEGYFMYUHOHGS-UHFFFAOYSA-N
InChI=1S/C7H14/c1-2-4-6-7-5-3-1/h1-7H2
| Molecular Formula | C7H14 |
| Molecular Weight | 98.1861 |
| 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 |
|---|---|---|
| Synthesis of enantiomerically pure, highly functionalized, medium-sized carbocycles from carbohydrates: formal total synthesis of (+)-calystegine b(2). | 2002 May 31 |
|
| The C7-C10 cycloalkanes revisited. | 2003 Nov 28 |
|
| Different forms of antiparallel stacking of hydrogen-bonded antidromic rings in the solid state: polymorphism with virtually the same unit cell and two-dimensional isostructurality with alternating layers. | 2004 Dec |
|
| Silylcuprates from allene and their reaction with alpha,beta-unsaturatedd nitriles and imines. Synthesis of silylated oxo compounds leading to cyclopentane and cycloheptane ring formation. | 2005 Aug 19 |
|
| Electronic structure, spectra, and magnetic circular dichroism of cyclohexa-, cyclohepta-, and cyclooctapyrrole. | 2005 Jul 4 |
|
| Concise synthesis of novel oxa-bridged compounds. | 2005 Sep 16 |
|
| Phenalenyl-based neutral radical molecular conductors: substituent effects on solid-state structures and properties. | 2007 Jun 6 |
|
| Synthesis of vinylcycloheptadienes by the nickel-catalyzed three-component [3 + 2 + 2] cocyclization. Application to the synthesis of polycyclic compounds. | 2009 May 1 |
|
| Sphaeroane and neodolabellane diterpenes from the red alga Sphaerococcus coronopifolius. | 2009 May 19 |
|
| Guaiane sesquiterpenes from seaweed Ulva fasciata Delile and their antibacterial properties. | 2010 Jun |
|
| Using a threading-followed-by-swelling approach to synthesize [2]rotaxanes. | 2010 Jun 18 |
|
| Preparation of a cycloheptane ring from a 1,2-diketone with high stereoselectivity. | 2010 Nov 19 |
|
| 1,3-Dimethyl-5,6,7,8-tetra-hydro-4H-cyclo-hepta-[c]thio-phene-4,8-dione. | 2010 Nov 20 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:50:47 GMT 2023
by
admin
on
Sat Dec 16 08:50:47 GMT 2023
|
| Record UNII |
VTZ53P34JA
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
VTZ53P34JA
Created by
admin on Sat Dec 16 08:50:47 GMT 2023 , Edited by admin on Sat Dec 16 08:50:47 GMT 2023
|
PRIMARY | |||
|
9265
Created by
admin on Sat Dec 16 08:50:47 GMT 2023 , Edited by admin on Sat Dec 16 08:50:47 GMT 2023
|
PRIMARY | |||
|
291-64-5
Created by
admin on Sat Dec 16 08:50:47 GMT 2023 , Edited by admin on Sat Dec 16 08:50:47 GMT 2023
|
PRIMARY | |||
|
5164
Created by
admin on Sat Dec 16 08:50:47 GMT 2023 , Edited by admin on Sat Dec 16 08:50:47 GMT 2023
|
PRIMARY | |||
|
DTXSID0074269
Created by
admin on Sat Dec 16 08:50:47 GMT 2023 , Edited by admin on Sat Dec 16 08:50:47 GMT 2023
|
PRIMARY | |||
|
59
Created by
admin on Sat Dec 16 08:50:47 GMT 2023 , Edited by admin on Sat Dec 16 08:50:47 GMT 2023
|
PRIMARY | |||
|
Cycloheptane
Created by
admin on Sat Dec 16 08:50:47 GMT 2023 , Edited by admin on Sat Dec 16 08:50:47 GMT 2023
|
PRIMARY | |||
|
206-030-2
Created by
admin on Sat Dec 16 08:50:47 GMT 2023 , Edited by admin on Sat Dec 16 08:50:47 GMT 2023
|
PRIMARY |