Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H14 |
| Molecular Weight | 134.2182 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC1=CC(CC)=CC=C1
InChI
InChIKey=AFZZYIJIWUTJFO-UHFFFAOYSA-N
InChI=1S/C10H14/c1-3-9-6-5-7-10(4-2)8-9/h5-8H,3-4H2,1-2H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Iminopropadienones from dioxanediones, isoxazolopyrimidinones, pyridopyrimidinones, and pyridopyrimidinium olates. | 2002 Nov 29 |
|
| Room-temperature Negishi cross-coupling of unactivated alkyl bromides with alkyl organozinc reagents utilizing a Pd/N-heterocyclic carbene catalyst. | 2005 Oct 14 |
|
| Two-dimensional hopping motion of encapsulated La atoms in silylated La(2)@C(80). | 2007 Jul 14 |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
205-511-4
Created by
admin on Fri Dec 15 19:40:54 GMT 2023 , Edited by admin on Fri Dec 15 19:40:54 GMT 2023
|
PRIMARY | |||
|
ZM2X7I1G8Y
Created by
admin on Fri Dec 15 19:40:54 GMT 2023 , Edited by admin on Fri Dec 15 19:40:54 GMT 2023
|
PRIMARY | |||
|
8864
Created by
admin on Fri Dec 15 19:40:54 GMT 2023 , Edited by admin on Fri Dec 15 19:40:54 GMT 2023
|
PRIMARY | |||
|
4082
Created by
admin on Fri Dec 15 19:40:54 GMT 2023 , Edited by admin on Fri Dec 15 19:40:54 GMT 2023
|
PRIMARY | |||
|
DTXSID1022003
Created by
admin on Fri Dec 15 19:40:54 GMT 2023 , Edited by admin on Fri Dec 15 19:40:54 GMT 2023
|
PRIMARY | |||
|
62102
Created by
admin on Fri Dec 15 19:40:54 GMT 2023 , Edited by admin on Fri Dec 15 19:40:54 GMT 2023
|
PRIMARY | |||
|
141-93-5
Created by
admin on Fri Dec 15 19:40:54 GMT 2023 , Edited by admin on Fri Dec 15 19:40:54 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD
