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Merck

192309

Sigma-Aldrich

3,3-二甲基氧杂环丁烷

98%

别名:

β,β-Dimethyloxetane, 3,3-Dimethyloxacyclobutane, 3,3-Dimethyloxetane, 3,3-Dimethyltrimethylene oxide

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About This Item

经验公式(希尔记法):
C5H10O
CAS号:
分子量:
86.13
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

98%

折射率

n20/D 1.399 (lit.)

bp

81 °C/765 mmHg (lit.)

密度

0.835 g/mL at 25 °C (lit.)

SMILES 字串

CC1(C)COC1

InChI

1S/C5H10O/c1-5(2)3-6-4-5/h3-4H2,1-2H3

InChI 密鑰

RVGLUKRYMXEQAH-UHFFFAOYSA-N

象形圖

FlameExclamation mark

訊號詞

Danger

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Flam. Liq. 2

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

15.8 °F - closed cup

閃點(°C)

-9 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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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)
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
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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