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3,4-Epoxytetrahydrofuran

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Products Intro: Product Name:3,4-Epoxytetrahydrofuran
CAS:285-69-8
Purity:98% Package:1Kg; 25Kgs; 100Kgs; tons
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CAS:285-69-8
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CAS:285-69-8
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CAS:285-69-8
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Products Intro: Product Name:3,4-Epoxytetrahydrofuran
CAS:285-69-8
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg

3,4-Epoxytetrahydrofuran manufacturers

3,4-Epoxytetrahydrofuran Basic information
Uses
Product Name:3,4-Epoxytetrahydrofuran
Synonyms:3,4-EPOXYTETRAHYDROFURAN;3,6-DIOXABICYCLO[3.1.0]HEXANE;3,4-EPOXYTETRAHYDROFURAN 96%;3,4-Epoxytetrahydrofurane;3,4-Epoxytetrahydrofuran, 98 %;3,4-Epoxy-THF;3,4-Diepoxytetrahydrofuran;3,4-Epoxytetrahydrofuran,96%
CAS:285-69-8
MF:C4H6O2
MW:86.09
EINECS:206-006-1
Product Categories:
Mol File:285-69-8.mol
3,4-Epoxytetrahydrofuran Structure
3,4-Epoxytetrahydrofuran Chemical Properties
Boiling point 44°C 10mm
density 1.237
refractive index 1.445-1.449
Fp >38℃
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Liquid
color Clear yellow
Water Solubility MODERATELY SOLUBLE
InChIInChI=1S/C4H6O2/c1-3-4(6-3)2-5-1/h3-4H,1-2H2
InChIKeyAIUTZIYTEUMXGG-UHFFFAOYSA-N
SMILESC12C(O1)COC2
CAS DataBase Reference285-69-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-10
Safety Statements 36/37/39-26-23-16-36/37/38
RIDADR 1993
Hazard Note Irritant
HazardClass 3
PackingGroup 
HS Code 29321900
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
ProviderLanguage
3,6-Dioxabicyclo[3.1.0]hexane English
ACROS English
3,4-Epoxytetrahydrofuran Usage And Synthesis
Uses3,6-Dioxabicyclo[3.1.0]hexane was a reagent used in making various degradable polymers from epoxides using a versatile dinuclear chromium catalyst.
Chemical Propertiesclear yellow liquid
Synthesis
2,5-Dihydrofuran

1708-29-8

3,4-Epoxytetrahydrofuran

285-69-8

Step 1: 85% m-chloroperoxybenzoic acid (mCPBA) (18.86 g, 0.093 mol) was slowly added to 150 mL of dichloromethane solution containing 2,5-dihydrofuran (5.04 g, 0.072 mol) at 0°C in an ice-water bath. The reaction mixture was stirred at room temperature for 48 hours. After completion of the reaction, the precipitate was removed by filtration. The filtrate was washed sequentially with saturated aqueous sodium bicarbonate, water and brine. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give a mixture of white solid and yellow oil (5.24 g, 84.6% yield).

References[1] Patent: WO2008/33562, 2008, A2. Location in patent: Page/Page column 53
[2] Patent: US2009/76005, 2009, A1. Location in patent: Page/Page column 23
[3] Bioorganic and Medicinal Chemistry, 2006, vol. 14, # 24, p. 8467 - 8487
[4] Patent: US5374416, 1994, A
[5] Patent: US2009/30212, 2009, A1. Location in patent: Page/Page column 15-16
3,4-Epoxytetrahydrofuran Preparation Products And Raw materials
Raw materials2,5-Dihydrofuran-->3-Chloroperoxybenzoic acid-->Tetrahydrofuran
Tag:3,4-Epoxytetrahydrofuran(285-69-8) Related Product Information
Hexane Tetrahydrofuran 2-Methyltetrahydrofuran POLY(TETRAHYDROFURAN) STANDARD 15000 CIMICIFUGOSIDE LINDERANE Actein 27-DEOXYACTEIN 4,9,11-trioxatetracyclo[5.3.1.0(2,6).0(8,10)]undecan-3-one 2,5-3,4-dianhydroaltritol 26-DEOXYCIMICIFUGOSIDE (2R,4R,5R)-2-ALLYLOXYMETHYL-4-DIMETHOXYMETHYL-3,6-DIOXA-BICYCLO[3.1.0]HEXANE lophotoxin POLY(TETRAHYDROFURAN) STANDARD 20000 3,4-Epoxytetrahydrofuran 4,5-DIMETHYL-5-HYDROXY-3-(METHOXYCARBONYL)-3,4-EPOXY-GAMMA-BUTYROLACTONE METHYL-2,3-ANHYDRO-5-O-(4-PHENYLBENZOYL)-BETA-D-LYXOFURANOSIDE 4-ETHYL-3-(METHOXYCARBONYL)-5-METHYL-3,4-GAMMA-BUTYROLACTONE

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