192309
3,3-Dimethyloxetane
98%
Synonym(s):
β,β-Dimethyloxetane, 3,3-Dimethyloxacyclobutane, 3,3-Dimethyloxetane, 3,3-Dimethyltrimethylene oxide
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About This Item
Empirical Formula (Hill Notation):
C5H10O
CAS Number:
Molecular Weight:
86.13
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
98%
refractive index
n20/D 1.399 (lit.)
bp
81 °C/765 mmHg (lit.)
density
0.835 g/mL at 25 °C (lit.)
functional group
ether
SMILES string
CC1(C)COC1
InChI
1S/C5H10O/c1-5(2)3-6-4-5/h3-4H2,1-2H3
InChI key
RVGLUKRYMXEQAH-UHFFFAOYSA-N
Related Categories
accessory
Product No.
Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
15.8 °F - closed cup
Flash Point(C)
-9 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Peter Billing et al.
The Journal of organic chemistry, 77(24), 11227-11231 (2012-11-16)
A novel one-step method for mildly converting cyclic ethers into dibromo compounds is reported. Alcohols, oximes, aldehydes, and ketones are known to react under Appel or Corey-Fuchs reaction conditions, but apparently these have never been applied to oxetanes or larger
Copolymerization of oxetane with 3, 3-dimethyloxetane-I. Reactivity parameters and microstructure of the copolymers.
Bucquoye M and Goethals EJ.
Eur. Polymer J., 14(5), 323-328 (1978)
Cyclic oligomers in the cationic polymerization of 3, 3-dimethyloxetane.
Bucquoye M and Goethals EJ.
Makromol. Chem., 179(7), 1681-1688 (1978)
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