Methyl (3R)-3-hydroxyhexanoate

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Reagent Code: #209400
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CAS Number 109053-86-3

science Other reagents with same CAS 109053-86-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 146.19 g/mol
Formula C₇H₁₄O₃
badge Registry Numbers
MDL Number MFCD30336670
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. Its hydroxyl and ester functional groups allow for versatile chemical modifications. Commonly employed in the synthesis of biologically active molecules, including antibiotics and anti-inflammatory agents. Also serves as an intermediate in the preparation of flavor and fragrance compounds due to its fruity, creamy aroma profile. Compatible with asymmetric synthesis techniques, making it valuable in the development of enantiomerically pure drugs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,200.00
inventory 250mg
10-20 days ฿38,400.00
inventory 1g
10-20 days ฿115,200.00

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Methyl (3R)-3-hydroxyhexanoate
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Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. Its hydroxyl and ester functional groups allow for versatile chemical modifications. Commonly employed in the synthesis of biologically active molecules, including antibiotics and anti-inflammatory agents. Also serves as an intermediate in the preparation of flavor and fragrance compounds due to its fruity, creamy aroma profile. Compatible with asymmetric synthesis techniques, makin

Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. Its hydroxyl and ester functional groups allow for versatile chemical modifications. Commonly employed in the synthesis of biologically active molecules, including antibiotics and anti-inflammatory agents. Also serves as an intermediate in the preparation of flavor and fragrance compounds due to its fruity, creamy aroma profile. Compatible with asymmetric synthesis techniques, making it valuable in the development of enantiomerically pure drugs.

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