(R)-4-(2-Hydroxyethyl)-2,2-dimethyl-1,3-dioxolane

≥94%(GC)

Reagent Code: #230281
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CAS Number 70005-89-9

science Other reagents with same CAS 70005-89-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 146.19 g/mol
Formula C₇H₁₄O₃
badge Registry Numbers
MDL Number MFCD02682966
thermostat Physical Properties
Boiling Point 110°C|25mmHg(lit.)
inventory_2 Storage & Handling
Density 1.05
Storage Room temperature, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals and fine chemicals. Its cyclic acetal structure provides stability and stereochemical control, making it valuable in asymmetric synthesis. Commonly employed in the preparation of bioactive molecules where the (R)-enantiomer is required for optimal activity. Also utilized in the development of prodrugs and protective group strategies due to its hydrolytic stability under basic conditions and selective deprotection under acidic conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿5,630.00
1g
10-20 days ฿13,600.00
(R)-4-(2-Hydroxyethyl)-2,2-dimethyl-1,3-dioxolane
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Used as a chiral building block in the synthesis of pharmaceuticals and fine chemicals. Its cyclic acetal structure provides stability and stereochemical control, making it valuable in asymmetric synthesis. Commonly employed in the preparation of bioactive molecules where the (R)-enantiomer is required for optimal activity. Also utilized in the development of prodrugs and protective group strategies due to its hydrolytic stability under basic conditions and selective deprotection under acidic conditions.

Used as a chiral building block in the synthesis of pharmaceuticals and fine chemicals. Its cyclic acetal structure provides stability and stereochemical control, making it valuable in asymmetric synthesis. Commonly employed in the preparation of bioactive molecules where the (R)-enantiomer is required for optimal activity. Also utilized in the development of prodrugs and protective group strategies due to its hydrolytic stability under basic conditions and selective deprotection under acidic conditions.

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