(R)-(-)-2-Hydroxypropyl p-toluenesulfonate, with the CAS number 103775-61-7, is an organic compound characterized by its chiral nature, featuring a hydroxyl group and a p-toluenesulfonate moiety. This compound is typically used as a chiral auxiliary in asymmetric synthesis, facilitating the production of enantiomerically enriched compounds. It exhibits good solubility in polar organic solvents, making it suitable for various chemical reactions. The presence of the p-toluenesulfonate group enhances its reactivity, particularly in nucleophilic substitution reactions. Additionally, the hydroxyl group contributes to its ability to form hydrogen bonds, influencing its physical properties such as boiling point and melting point. The compound's chirality is significant in pharmaceutical applications, where the specific enantiomer can have distinct biological activities. Safety data indicates that, like many sulfonate esters, it should be handled with care, as it may cause irritation upon contact with skin or eyes. Overall, (R)-(-)-2-hydroxypropyl p-toluenesulfonate is a valuable reagent in synthetic organic chemistry.

(R)-(-)-2-HYDROXYPROPYL P-TOLUENESULFONATE

103775-61-7: (R)-(-)-2-Hydroxypropyl p-toluenesulfonate, with the CAS number 103775-61-7, is an organic compound characterized by its chiral nature, featuring a hydroxyl group and a p-toluenesulfonate moiety. This compound is typically used as a chiral auxiliary in asymmetric synthesis, facilitating the production of enantiomerically enriched compounds. It exhibits good solubility in polar organic solvents, making it suitable for various chemical reactions. The presence of the p-toluenesulfonate group enhances its reactivity, particularly in nucleophilic substitution reactions. Additionally, the hydroxyl group contributes to its ability to form hydrogen bonds, influencing its physical properties such as boiling point and melting point. The compound's chirality is significant in pharmaceutical applications, where the specific enantiomer can have distinct biological activities. Safety data indicates that, like many sulfonate esters, it should be handled with care, as it may cause irritation upon contact with skin or eyes. Overall, (R)-(-)-2-hydroxypropyl p-toluenesulfonate is a valuable reagent in synthetic organic chemistry.

(R)-(-)-2-Hydroxypropyl P-Toluenesulfonate

(R)-2-hydroxypropyl 4-methylbenzenesulfonate

CAS 103775-61-7

(R)-(-)-2-HYDROXYPROPYL P-TOLUENESULFONATE

(R)-(-)-2-Hydroxypropyl P-Toluenesulfonate

Ref: IN-DA009SLU

(R)-2-hydroxypropyl 4-methylbenzenesulfonate

Ref: 54-OR91978

(R)-2-hydroxypropyl 4-methylbenzenesulfonate

Ref: 10-F982689