107473-33-6
107473-33-6 structure
- Name: 2-Phenylethanol-d4
- Chemical Name: 2-phenylethan-1,1,2,2-d4-ol
- CAS Number: 107473-33-6
- Molecular Formula: C8H6D4O
- Molecular Weight: 126.18900
- Catalog: Signaling Pathways Anti-infection Bacterial
- Create Date: 2018-09-26 11:40:57
- Modify Date: 2024-01-04 00:36:44
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2-Phenylethanol-d4 is the deuterium labeled 2-Phenylethanol[1]. 2-Phenylethanol (Phenethyl alcohol), extracted from rose, carnation, hyacinth, Aleppo pine, orange blossom and other organisms, is a colourless liquid. It has a pleasant floral odor and also an autoantibiotic produced by the fungus Candida albicans[2]. It is used as an additive in cigarettes and also used as a preservative in soaps due to its stability in basic conditions.
| Name | 2-phenylethan-1,1,2,2-d4-ol |
|---|---|
| Synonyms |
1,1,2,2-tetradeuterio-2-phenyl-ethanol
2-phenylethyl mercaptan 1,2-phenylethylmercaptane Benzeneethanethiol 2-phenylethanol-1,1,2,2-d4 Phenethyl mercaptan 2-phenyl-ethanethiol Phenylethyl mercaptan 2-mercaptophenylethane 1.1.2.2-Tetradeutero-2-phenylethylalkohol 2-phenyl-1-ethanethiol |
| Description | 2-Phenylethanol-d4 is the deuterium labeled 2-Phenylethanol[1]. 2-Phenylethanol (Phenethyl alcohol), extracted from rose, carnation, hyacinth, Aleppo pine, orange blossom and other organisms, is a colourless liquid. It has a pleasant floral odor and also an autoantibiotic produced by the fungus Candida albicans[2]. It is used as an additive in cigarettes and also used as a preservative in soaps due to its stability in basic conditions. |
|---|---|
| Related Catalog | |
| In Vitro | Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1]. |
| References |
| Molecular Formula | C8H6D4O |
|---|---|
| Molecular Weight | 126.18900 |
| Exact Mass | 126.09800 |
| PSA | 20.23000 |
| LogP | 1.22140 |
|
~%
107473-33-6 |
| Literature: AUSPEX PHARMACEUTICALS, INC. Patent: US2010/16365 A1, 2010 ; Location in patent: Page/Page column 20 ; US 20100016365 A1 |
|
~%
107473-33-6 |
| Literature: Gessner, Uwe; Heesing, Albert Chemische Berichte, 1985 , vol. 118, # 7 p. 2593 - 2606 |
|
~%
107473-33-6 |
| Literature: Gessner, Uwe; Heesing, Albert Chemische Berichte, 1985 , vol. 118, # 7 p. 2593 - 2606 |
| Precursor 3 | |
|---|---|
| DownStream 0 | |