Detail of > 764-99-8
- MSDS Download

- CAS Number:
- 764-99-8
- Name:
Ethene,1,1'-[oxybis(2,1-ethanediyloxy)]bis-
- Superlist Name:
- Diethylene glycol divinyl ether
- Formula:
- C8H14O3
- Molecular Structure:
![Molecular Structure of 764-99-8 (Ethene,1,1'-[oxybis(2,1-ethanediyloxy)]bis-)](http://www.lookchem.com/300w/2010/0624/764-99-8.jpg)
- Synonyms:
- Ether,bis[2-(vinyloxy)ethyl] (6CI,7CI,8CI);3,6,9-Trioxaundeca-1,10-diene;Bis[2-(vinyloxy)ethyl] ether;DEGV;Divinylcarbitol;NSC 6117;Rapi-Cure DVE 2;{2-[2-(ethenyloxy)ethoxy]ethoxy}ethene;1-ethenoxy-2-(2-ethenoxyethoxy)ethane;
- Molecular Weight:
- 158.22
- EINECS:
- 212-133-3
- Density:
- 0.931 g/cm3
- Melting Point:
- -21 °C
- Boiling Point:
- 195.4 °C at 760 mmHg
- Flash Point:
- 62.2 °C
- Risk Codes:
- 36/38
- Safety:
- 26-36Details
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Reference
- Copolymerization of divinyl ethers with maleic anhydride
- Copolymerization of divinyl ethers with maleic anhydride. Tsarik, L. Ya.; Mantsivoda, G. P.; Ratovskii, G. V.; Dmitrieva, T. V.; Kalabina, A. V. (Irkutsk. Gos. Univ., Irkutsk, USSR). Vysokomol. Soedin., Ser. B, 19(8), 601-4 (Russian) 1977. CODEN: VYSBAI. DOCUMENT TYPE: Journal CA Section: 35 (Synthetic High Polymers) The copolymn. of hydroquinone divinyl ether (I) [4024-21-9] and diethylene glycol divinyl ether (II) [764-99-8] with maleic anhydride (III) [108-31-6] at 60.degree. in the presence of AIBN occurred via donor-acceptor complex formation and had highest conversion at 2:1 III-II ratio and 1.3-1.5:1 III-I ratio. The reactivity ratios were rIII = 0.14 .+-. 0.037, rII = 0.01 .+-. 0.003 and rIII = 0.165 .+-. 0.061, rI = 0 .+-. 0.07, which indicates the formation of alternating copolymers. The copolymers had a 3-dimensional structure and were insol., but swelled in org. solvents (60-70% in Me2CO; 80-100% in dioxane). Hydrolysis of the copolymers gave a CO2H-contg. cation exchanger having exchange capacity 8-10 mequiv/g (0.1N KOH).
- Modification of oligodiene diols with divinyl ether of diethylene glycol
- Modification of oligodiene diols with divinyl ether of diethylene glycol. Tsitokhtsev, V. A.; Nikitina, N. A.; Markelova, L. I.; Smirnova, V. K. (USSR). Kauch. Rezina, (8), 19-22 (Russian) 1986. CODEN: KCRZAE. ISSN: 0022-9466. DOCUMENT TYPE: Journal CA Section: 39 (Synthetic Elastomers and Natural Rubber) The kinetics of the interaction of diethylene glycol divinyl ether [764-99-8] with oligodiene rubber diols (e.g. OH group-terminated butadiene-isoprene copolymer) in the presence of HCl in dioxane solns. and trifluoroacetic acid [76-05-1] catalysts was studied for the synthesis of oligodiene acetals (OA) with reactive end groups. The OA have high compatibility with rubber and can be used in polymer composites. The synthesis of OA with oxyvinyl end groups can be controlled by varying the conditions of the reaction between the diethylene glycol divinyl ether and oligodiene diol.
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