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ChemicalBook--->CAS DataBase List--->32233-43-5

32233-43-5

32233-43-5 Structure

32233-43-5 Structure
IdentificationBack Directory
[Name]

(4S)-(+)-4-(2-HYDROXYETHYL)-2,2-DIMETHYL-1,3-DIOXOLANE
[CAS]

32233-43-5
[Synonyms]

(S)-(+)-2,2-Dimethyl-1,3-Dio
(S)-1,2-ISOPROPYLIDENEBUTANE-1,2,4-TRIOL
(4S)-(+)-4-(2-HYDROXYETHYL)-2,2-DIMETHY&
(4S)-2,2-Dimethyl-1,3-Dioxolane-4-Ethanol
1,3-dioxolane-4-ethanol,2,2-dimethyl-,(4s)
(S)-1,2-O-Isopropylidenebutane-1,2,4-triole
2-(2,2-diMethyl-1,3-dioxolan-4-yl)ethan-1-ol
(s)-(+)-2,2-dimethyl-1,3-dioxolane-4-ethanol
2-(4S)-2,2-Dimethyl-1,3-dioxolan-4-ylethanol
2-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]ethanol
(S)-2,2-DIMETHYL-4-HYDROXYETHYL-[1,3]DIOXOLANE
(4S)-(2,2-DIMETHYL-[1,3]DIOXOLAN-4-YL)-ETHANOL
(S)-2-(2,2-Dimethyl-[1,3]dioxolan-4-yl)ethanol
2(2,2-DIMETHYL-[1,3] DIOXOLAN-4-YL)-ETHANOL (S)
(S)-2-(2,2-dimethyl-1,3-dioxolan-4-yl)ethan-1-ol
(S)-4-(2-Hydroxyethyl)-2,2-dimethyl-1,3-dioxolane
2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]ethan-1-ol
(S)-4-(2-Hydroxyethyl)-2,2-dimethyl-1,3-dioxolane>
(4S)-(+)-4-(2-HYDROXYETHYL)-2,2-DIMETHYL-1,3-DIOXOLANE
(4S)-(+)-4-(2-Hydroxyethyl)-2,2-dimenthyl-1,3-dioxolane
(S)-4-(2-Hydroxyethyl)-2,2-dimethyl-1,3-dioxolane
(4S)-(+)-4-(2-Hydroxyethyl)-2,2-diMethyl-1,3-dioxolane 96%
[Molecular Formula]

C7H14O3
[MDL Number]

MFCD02682967
[MOL File]

32233-43-5.mol
[Molecular Weight]

146.18
Chemical PropertiesBack Directory
[Boiling point ]

98 °C15 mm Hg(lit.)
[density ]

1.027 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.4380(lit.)
[Fp ]

213 °F
[storage temp. ]

2-8°C
[form ]

liquid
[pka]

14.80±0.10(Predicted)
[color ]

Colorless to Almost colorless
[optical activity]

[α]20/D +2°, c = 1% in chloroform
[InChIKey]

LMHCQSYOFZFRMI-AGZQWMCOSA-N
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[HS Code ]

2932.99.9090
Hazard InformationBack Directory
[Uses]

(4S)-(+)-4-(2-Hydroxyethyl)-2,2-dimethyl-1,3-dioxolane may be used in the preparation (prop-2-ynyloxy)ethyl-tethered dioxolanes via O-propargylation. It may also be used as an intermediate in the total synthesis of rugulactone.
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