(S)-(-)-4-Chloromethyl-2,2-dimethyl-1,3-dioxolane

98%

Reagent Code: #234250
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CAS Number 60456-22-6

science Other reagents with same CAS 60456-22-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.6 g/mol
Formula C₆H₁₁ClO₂
badge Registry Numbers
MDL Number MFCD00273365
thermostat Physical Properties
Boiling Point 63 °C37 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.103 g/mL at 25 °C(lit.)
Storage Room temperature, flammable area

description Product Description

Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals where stereochemistry plays a critical role. Its protected diol functionality and reactive chloromethyl group allow selective transformations, making it valuable in asymmetric synthesis. Commonly employed in the preparation of side chains for beta-lactam antibiotics and other medicinally relevant molecules. Also utilized in agrochemicals and fine chemicals for introducing chiral centers during development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿180.00
inventory 5g
10-20 days ฿540.00
inventory 25g
10-20 days ฿1,990.00
inventory 100g
10-20 days ฿7,530.00
(S)-(-)-4-Chloromethyl-2,2-dimethyl-1,3-dioxolane
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Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals where stereochemistry plays a critical role. Its protected diol functionality and reactive chloromethyl group allow selective transformations, making it valuable in asymmetric synthesis. Commonly employed in the preparation of side chains for beta-lactam antibiotics and other medicinally relevant molecules. Also utilized in agrochemicals and fine chemicals for introducing chiral centers duri

Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals where stereochemistry plays a critical role. Its protected diol functionality and reactive chloromethyl group allow selective transformations, making it valuable in asymmetric synthesis. Commonly employed in the preparation of side chains for beta-lactam antibiotics and other medicinally relevant molecules. Also utilized in agrochemicals and fine chemicals for introducing chiral centers during development.

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