Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H12 |
| Molecular Weight | 132.2023 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C=CCCC1=CC=CC=C1
InChI
InChIKey=PBGVMIDTGGTBFS-UHFFFAOYSA-N
InChI=1S/C10H12/c1-2-3-7-10-8-5-4-6-9-10/h2,4-6,8-9H,1,3,7H2
| Molecular Formula | C10H12 |
| Molecular Weight | 132.2023 |
| 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 |
|---|---|---|
| Gas-phase pyrolytic reaction of 4-aryl-3-buten-2-ols and allyl benzyl ethers: kinetic and mechanistic study. | 2010-01-20 |
|
| Dimethyl (2-hydr-oxy-4-phenyl-but-3-en-2-yl)phospho-nate. | 2009-10-31 |
|
| Synthesis of (+)-CP-99,994 via Pd(0)-catalyzed asymmetric allylic and homoallylic C-H Diamination of terminal olefin. | 2009-10-02 |
|
| Asymmetric [2,3]-wittig rearrangement of oxygenated allyl benzyl ethers in the presence of a chiral di-tBu-bis(oxazoline) ligand: a novel synthetic approach to THF lignans. | 2009-09-28 |
|
| Isolation and functional analysis of cytochrome P450 CYP153A genes from various environments. | 2005-12 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:22:50 GMT 2025
by
admin
on
Mon Mar 31 19:22:50 GMT 2025
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| Record UNII |
58584HOZ1Z
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| Record Status |
Validated (UNII)
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| Record Version |
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