(R)-sec-Butyl 4-methylbenzenesulfonate

97%

Reagent Code: #231797
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CAS Number 61530-30-1

science Other reagents with same CAS 61530-30-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.31 g/mol
Formula C₁₁H₁₆O₃S
badge Registry Numbers
MDL Number MFCD03093936
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used primarily as a chiral intermediate in organic synthesis, particularly in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. Its sulfonate group acts as a good leaving group, making it suitable for nucleophilic substitution reactions. The presence of the chiral center allows for stereoselective transformations, which are valuable in asymmetric synthesis. Commonly employed in the development of active pharmaceutical ingredients where control of stereochemistry is critical for biological activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿13,580.00
250mg
10-20 days ฿23,050.00
1g
10-20 days ฿65,450.00
(R)-sec-Butyl 4-methylbenzenesulfonate
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Used primarily as a chiral intermediate in organic synthesis, particularly in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. Its sulfonate group acts as a good leaving group, making it suitable for nucleophilic substitution reactions. The presence of the chiral center allows for stereoselective transformations, which are valuable in asymmetric synthesis. Commonly employed in the development of active pharmaceutical ingredients where control of stereochemistry is critical for

Used primarily as a chiral intermediate in organic synthesis, particularly in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. Its sulfonate group acts as a good leaving group, making it suitable for nucleophilic substitution reactions. The presence of the chiral center allows for stereoselective transformations, which are valuable in asymmetric synthesis. Commonly employed in the development of active pharmaceutical ingredients where control of stereochemistry is critical for biological activity.

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