tert-Butyl(R)-3-hydroxybutanoate

98%

Reagent Code: #154991
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CAS Number 110171-06-7

science Other reagents with same CAS 110171-06-7

blur_circular Chemical Specifications

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Weight 160.21 g/mol
Formula C₈H₁₆O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals and fine chemicals. Its enantiomerically pure form makes it valuable for producing optically active compounds, particularly in the development of antibiotics, antifungals, and cholesterol-lowering agents like statins. Commonly employed in asymmetric synthesis to introduce hydroxy ester functionality with high stereocontrol. Also utilized in the preparation of biodegradable polymers and as an intermediate in flavor and fragrance manufacturing due to its ability to form lactones.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,100.00
inventory 250mg
10-20 days ฿10,370.00
inventory 1g
10-20 days ฿27,960.00

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tert-Butyl(R)-3-hydroxybutanoate
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Used as a chiral building block in the synthesis of pharmaceuticals and fine chemicals. Its enantiomerically pure form makes it valuable for producing optically active compounds, particularly in the development of antibiotics, antifungals, and cholesterol-lowering agents like statins. Commonly employed in asymmetric synthesis to introduce hydroxy ester functionality with high stereocontrol. Also utilized in the preparation of biodegradable polymers and as an intermediate in flavor and fragrance manufactu

Used as a chiral building block in the synthesis of pharmaceuticals and fine chemicals. Its enantiomerically pure form makes it valuable for producing optically active compounds, particularly in the development of antibiotics, antifungals, and cholesterol-lowering agents like statins. Commonly employed in asymmetric synthesis to introduce hydroxy ester functionality with high stereocontrol. Also utilized in the preparation of biodegradable polymers and as an intermediate in flavor and fragrance manufacturing due to its ability to form lactones.

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