3,6-Dioxabicyclo[3.1.0]hexane

Product Information

Molecular Formula:
C4H6O2
Molecular Weight:
86.09
Description
3,6-Dioxabicyclo[3.1.0]hexane (CAS# 285-69-8 ) is a useful research chemical.
Synonyms
3,4-Epoxytetrahydrofuran; 3,6-Dioxabicyclo(3.1.0)hexane; MFCD00800639
IUPAC Name
3,6-dioxabicyclo[3.1.0]hexane
Canonical SMILES
C1C2C(O2)CO1
InChI
InChI=1S/C4H6O2/c1-3-4(6-3)2-5-1/h3-4H,1-2H2
InChI Key
AIUTZIYTEUMXGG-UHFFFAOYSA-N
Boiling Point
144 ℃
Flash Point
50 ℃
Purity
> 97.0 % (GC)
Density
1.20 g/cm3
Appearance
Colorless to light yellow clear liquid
Refractive Index
1.44

Safety Information

Hazards
H226:
Flammable liquid and vapour.
Precautionary Statement
P210:
Keep away from heat, sparks, open flames, hot surfaces. No smoking.
P233:
Keep container tightly closed.
P303+P361+P353:
IF ON SKIN (or hair):
Take off immediately all contaminated clothing. [As modified by IV ATP].
Rinse skin with water/shower.
P370+P378:
In case of fire:
Use for extinction:
P403+P235:
Store in a well ventilated place.
Keep cool.
P501:
Dispose of contents/container in accordance with local/regional/national/international regulations.
Signal Word
Warning

Computed Properties

XLogP3
-0.4
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
0
Exact Mass
86.036779430 g/mol
Monoisotopic Mass
86.036779430 g/mol
Topological Polar Surface Area
21.8Ų
Heavy Atom Count
6
Formal Charge
0
Complexity
63.9
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
2
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-113105611-A Polymerization method for ring-opening alternating copolymerization of anhydride compound and epoxy compound 2021-05-28
CN-113264908-A Preparation method of hydroxyl tetrahydrofuran compound 2021-05-26
CN-112371153-A Bimetallic CoNi-ZIF derived CoNi @ CN catalyst, preparation method and catalytic hydrogenation application thereof 2020-11-03
WO-2022051337-A1 2-aminoquinazolines as lrrk2 inhibitors, pharmaceutical compositions, and uses thereof 2020-09-02
CN-111978531-A Cellulose grafted full-biodegradable high polymer material and preparation method thereof 2020-08-26
US-2022048909-A1 Heteroaryl substituted spiropiperidinyl derivatives and pharmaceutical uses thereof 2020-08-14
WO-2022034529-A1 Heteroaryl substituted spiropiperidinyl derivatives and pharmaceutical uses thereof 2020-08-14
CN-113817388-A Liquid containing conductive polymer, conductive film, conductive laminate, and method for producing same 2020-06-18
JP-2021138012-A Coating film manufacturing method, partially conductive coating film and its manufacturing method, laminated film and its manufacturing method, conductive resin circuit and its manufacturing method, and circuit film 2020-03-03
WO-2021173523-A1 Hot melt extruded solid dispersions containing a bcl2 inhibitor 2020-02-24

Literatures

PMID Publication Date Title Journal
20485829 2010-07-07 A stereocontrolled method for the synthesis of D- and L-2-deoxy-C-nucleosides using an intramolecular Sakurai-type cyclisation reaction Chemical communications (Cambridge, England)
12926388 2003-04-07 Enantioselective alkylative double ring-opening of epoxides derived from cyclic allylic ethers: synthesis of enantioenriched unsaturated diols Organic & biomolecular chemistry
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Related Products

Online Inquiry
  • Verification code
USA
  • International:
  • US & Canada (Toll free):
  • Email:
  • Fax:
UK
  • Email:
Copyright © 2024 BOC Sciences. All rights reserved.
Inquiry Basket