(1R,2S,5R)-(-)-MENTHYL (S)-P-TOLUENESULFINATE - Names and Identifiers
Name | (-)-(1R)-menthyl (S)-toluene-4-sulfinate
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Synonyms | ()-(1R)-Menthyl (S)-p-toluenesulfinate (-)-(1R)-menthyl (S)-toluene-4-sulfinate (1R,2S,5R)-()-Menthyl (S)-p-toluenesulfinate (1r,2s,5r)-(-)-menthyl (s)-p-toluenesulfinate p-Toluenesulfinic acid (1R,3R,4S)-menthyl ester p-Toluenesulfinic acid (1R,3R,4S)-p-menthane-3-yl ester 4-Methylbenzenesulfinic acid (1R,3R,4S)-p-menthane-3-yl ester p-Toluenesulfinic acid (1R,1β)-2α-isopropyl-5β-methylcyclohexyl ester p-Toluenesulfinic acid (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl ester (1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl 4-methylbenzenesulfinate (S)-(-)-Menthyl p-toluenesulfinate, (-)-(1R)-Menthyl (S)-p-toluenesulfinate 4-Methylbenzenesulfinic acid (1R)-2α-isopropyl-5β-methylcyclohexane-1β-yl ester
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CAS | 1517-82-4
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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?/m1/s1 |
(1R,2S,5R)-(-)-MENTHYL (S)-P-TOLUENESULFINATE - Physico-chemical Properties
Molecular Formula | C17H26O2S
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Molar Mass | 294.45 |
Density | 1.08 |
Melting Point | 99-104°C |
Boling Point | 402.3±38.0 °C(Predicted) |
Flash Point | 197.13°C |
Solubility | Acetone (Slightly), Chloroform (Slightly) |
Vapor Presure | 0mmHg at 25°C |
Appearance | White crystalline powder |
Color | Yellow to brown or gray |
BRN | 3207468 |
Storage Condition | -20°C |
Sensitive | Sensitive to heat |
Refractive Index | -199 ° (C=1.5, Aceto |
MDL | MFCD00010192 |
(1R,2S,5R)-(-)-MENTHYL (S)-P-TOLUENESULFINATE - Risk and Safety
Safety Description | S22 - Do not breathe dust.
S24/25 - Avoid contact with skin and eyes.
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WGK Germany | 3 |
HS Code | 29309090 |
(1R,2S,5R)-(-)-MENTHYL (S)-P-TOLUENESULFINATE - Introduction
(-)-(1R)-menthyl (S)-toluene-4-sulfinate is an organic compound whose chemical structure is arranged as 1R,2S,5R. Its chemical nature is solid and has a strong aroma.
The main use of this compound is as a chiral catalyst and synthetic intermediate. It is widely used in asymmetric synthesis reactions in the field of organic synthesis, especially in the fields of pharmaceuticals, pesticides and materials chemistry. It can aid in the synthesis of compounds with high stereoselectivity.
For the preparation of (-)-(1R)-menthyl (S)-toluene-4-sulfinate, a commonly used method is synthesis through stereoselective chemical reactions. The specific preparation method can be adjusted according to specific requirements and reaction conditions.
Regarding safety information, the use of chemicals needs to be operated according to correct operation and protective measures. For the storage of chemicals, corresponding regulations should be observed to ensure their safety, stability and no pollution to the environment. At the same time, when using the compound, the relevant operating instructions should be followed, and care should be taken to avoid contact with the skin, inhalation and ingestion. When any chemical is used, it should be guarded and handled in accordance with the safety data sheets and guidelines provided. It is recommended to consult relevant professionals and read detailed chemical safety information before use.
Last Update:2024-04-09 21:11:58