5-ENDO-METHOXYCARBONYL-2-NORBORNENE
Compound with spectra: 2 NMR, and 5 MS (GC)
| SpectraBase Compound ID | 4hpisshp53g |
|---|---|
| InChI | InChI=1S/C9H12O2/c1-11-9(10)8-5-6-2-3-7(8)4-6/h2-3,6-8H,4-5H2,1H3/t6-,7+,8-/m1/s1 |
| InChIKey | RMAZRAQKPTXZNL-GJMOJQLCSA-N |
| Mol Weight | 152.19 g/mol |
| Molecular Formula | C9H12O2 |
| Exact Mass | 152.08373 g/mol |
| Enantiomer InChIKey | RMAZRAQKPTXZNL-RNJXMRFFSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | HE-1982-0-0 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | NW-1586-0-0 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | AD-0-2532-0 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | AD-0-2532-0 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | Unknown |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- BICYCLO-[2.2.1]-HEPT-5-EN-2-ENDO-CARBOXYLIC-ACID,METHYLESTER
- 5-bicyclo[2.2.1]hept-2-enecarboxylic acid methyl ester
1-(5-bicyclo[2.2.1]hept-2-enyl)-2-hydroxy-ethanone
Bicyclo[2.2.1]hept-2-ene-5-yl, vinyl ketone
BICYCLO[2.2.2]OCT-5-ENE-exo-2-CARBOXYLIC ACID
endo-BICYCLO[2.2.2]OCT-5-ENE-2-CARBOXYLIC ACID
BICYCLO-[2.2.2]-OCT-5-EN-2-ENDO-CARBONSAEURE
BICYCLO-[2.2.2]-OCT-5-EN-2-EXO-CARBONSAEURE
BICYCLO-[2.2.2]-OCT-2-EN-5-OXO-CARBOXYLIC-ACID
Methyl cis-(5-Carbomethoxy-1-cyclohexen-3-yl)acetate
Methyl trans-(5-Carbomethoxy-1-cyclohexen-3-yl)acetate
2-[(1R,4S)-4-hydroxy-1-cyclopent-2-enyl]propanedioic acid dimethyl ester
| Title | Journal or Book | Year |
|---|---|---|
| The Reaction of 5-Substituted-2-Norbornenes with Phenylselenyl Chloride | Australian Journal of Chemistry | 2008 |
| Stereoselection in thermal asymmetric Diels-Alder reactions. Electronic vs. steric effects | The Journal of Organic Chemistry | 1992 |
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