(+)-(1S)-menthyl (R)-toluene-4-sulfinate
(+)-(1S)-menthyl (R)-toluene-4-sulfinate
CAS: 91796-57-5
Molecular Formula: C17H26O2S
(+)-(1S)-menthyl (R)-toluene-4-sulfinate - Names and Identifiers
| Name | (+)-(1S)-menthyl (R)-toluene-4-sulfinate |
| Synonyms | (R)-(+)-MENTHYL P-TOLUENESULFINATE (+)-(1S)-Menthyl (R)-p-toluenesulfinate (+)-(1S)-menthyl (R)-toluene-4-sulfinate (+)-(1S)-MENTHYL (R)-TOLUENE-4-SULFINATE (1S,2R,5S)-MENTHYL (R)-P-TOLUENESULFINATE (1S,2R,5S)-(+)-MENTHYL (R)-P-TOLUENESULFINATE (1s,2r,5s)-(+)-menthyl (r)-p-toluenesulfinate (R)-(+)-P-TOLUENESULFINIC ACID D-MENTHYL ESTER (R)-(5S)-2-Isopropyl-5-methylcyclohexyl 4-methylbenzenesulfinate p-Toluenesulfinic acid (1R)-5β-methyl-2β-isopropylcyclohexan-1β-yl ester |
| CAS | 91796-57-5 |
| InChI | InChI=1/C17H26O2S/c1-12(2)16-10-7-14(4)11-17(16)19-20(18)15-8-5-13(3)6-9-15/h5-6,8-9,12,14,16-17H,7,10-11H2,1-4H3/t14-,16?,17?,20?/m0/s1 |
(+)-(1S)-menthyl (R)-toluene-4-sulfinate - Physico-chemical Properties
| Molecular Formula | C17H26O2S |
| Molar Mass | 294.45 |
| Melting Point | 104-106°C(lit.) |
| Appearance | powder to crystal |
| Color | White to Almost white |
| BRN | 4907352 |
| Storage Condition | 2-8°C |
| Refractive Index | 200 ° (C=2, Acetone) |
(+)-(1S)-menthyl (R)-toluene-4-sulfinate - Risk and Safety
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
(+)-(1S)-menthyl (R)-toluene-4-sulfinate - Introduction
()-(1S)-menthyl (R)-toluene-4-sulfinate is an organic compound with a cool, minty odor. Its chemical formula is C10H12O2S and its molecular weight is 196.27. It is a solid, soluble in organic solvents such as ethanol and ether.
This compound is commonly used in the synthesis of chiral compounds and pharmaceutical intermediates. It is a chiral menthol, and chiral molecules have important applications in the pharmaceutical and fragrance industries. It can be used as a chiral inducer, catalyst and substrate for resolution enzymes.
The method for preparing ()-(1S)-menthyl (R)-toluene-4-sulfinate is obtained by reacting menthol with p-toluenesulfonyl chloride. Specific synthetic methods can be found in the organic synthesis literature for the synthesis of organic compounds.
For safety information,( )-(1S)-menthyl (R)-toluene-4-sulfinate is a chemical and should be used in accordance with safe operating procedures. It may be irritating to the eyes, skin and respiratory system. When in use, wear appropriate personal protective equipment to avoid inhalation or contact with skin and eyes. In case of accidental contact or discomfort, please seek medical attention. Follow the relevant safety guidelines when storing and handling.
This compound is commonly used in the synthesis of chiral compounds and pharmaceutical intermediates. It is a chiral menthol, and chiral molecules have important applications in the pharmaceutical and fragrance industries. It can be used as a chiral inducer, catalyst and substrate for resolution enzymes.
The method for preparing ()-(1S)-menthyl (R)-toluene-4-sulfinate is obtained by reacting menthol with p-toluenesulfonyl chloride. Specific synthetic methods can be found in the organic synthesis literature for the synthesis of organic compounds.
For safety information,( )-(1S)-menthyl (R)-toluene-4-sulfinate is a chemical and should be used in accordance with safe operating procedures. It may be irritating to the eyes, skin and respiratory system. When in use, wear appropriate personal protective equipment to avoid inhalation or contact with skin and eyes. In case of accidental contact or discomfort, please seek medical attention. Follow the relevant safety guidelines when storing and handling.
Last Update：2024-04-09 20:02:46
