(S)-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol

(S)-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol
  • CAS No.:22323-82-6
Other grades of this product :
(S)-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol Basic information
Product Name:(S)-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol
Synonyms:1,3-Dioxolane-4-methanol, 2,2-dimethyl-, (S)-;(S)-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol,98%;(4S)-(+)-2,2-Dimethyl-4-(hydroxymethyl)-1,3-dioxolane 98%;(S)-(+)-1,2-Isopropylideneglycerol, [(4S)-(+)-2,2-Dimethyl-1,3-dioxolan-4-yl]methanol, (S)-Solketal;(S)-(+)-2,2-DiMethyl-1,3-Dioxalane-4-Methanol;(S)-(+)-2,2-DiMethyl-1,3-dioxolane-4-Methanol, 98% 5GR;D-1,2-O-ISOPROPYLIDENE-SN-GLYCEROL;D-(+)-1,2-ISOPROPYLIDENEGLYCEROL
CAS:22323-82-6
MF:C6H12O3
MW:132.16
EINECS:244-910-8
Product Categories:Miscellaneous;Inhibitors;pharmacetical;Chiral Reagent;Chiral Reagents;Chiral Building Blocks;Dioxanes & Dioxolanes;Dioxolanes;Glycidyl Compounds, etc. (Chiral);Synthetic Organic Chemistry;Heterocycles
Mol File:22323-82-6.mol
(S)-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol Chemical Properties
alpha 11 º (c=5, CH3OH)
Boiling point 82-83 °C14 mm Hg(lit.)
density 1.07 g/mL at 25 °C(lit.)
refractive index n20/D 1.434
Fp 176 °F
storage temp. 2-8°C
solubility Chloroform, Ethanol, Methanol
form Liquid
pka14.20±0.10(Predicted)
color Clear colorless to light yellow
Specific Gravity1.07
optical activity[α]20/D +13.5°, neat
Water Solubility miscible
Merck 14,5213
BRN 80118
Stability:Stable. Flammable. Incompatible with oxidizing agents.
InChIKeyRNVYQYLELCKWAN-YFKPBYRVSA-N
CAS DataBase Reference22323-82-6(CAS DataBase Reference)
NIST Chemistry ReferenceL-Acetone glycerol(22323-82-6)
Safety Information
Safety Statements 23-24/25
WGK Germany 3
RTECS JI0400000
10
HS Code 29329970
MSDS Information
ProviderLanguage
(+)-2,3-O-Isopropylidene-sn-glycerol English
ACROS English
SigmaAldrich English
ALFA English
(S)-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol Usage And Synthesis
Chemical PropertiesColorless Oil
Uses(S)-(+)-2,3-O-Isopropylideneglycerol acts as a MEK inhibitor with antitumor activity. It is also employed in the preparation of a chiral allylic triol through extrusion of sulfur dioxide from an alfa,beta-epoxysulfone.
UsesA MEK inhibitor with antitumor activity
General Description(S)-(+)-1,2-Isopropylideneglycerol is a key building block for the synthesis of glycerides and of phosphoglycerides.

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