三乙烯基环三硼氧烷

三乙烯基环三硼氧烷
	IUPAC名; 2,4,6-tris(ethenyl)-1,3,5,2,4,6-trioxatriborinane
别名	Trivinylboroxin, triethenylboroxin, 2,4,6-trivinyl-1,3,5,2,4,6-trioxatriborinane, 2,4,6-trivinylcyclotriboroxane
识别
CAS号	92988-08-4
PubChem	2734807
ChemSpider	2016551
SMILES	B1(OB(OB(O1)C=C)C=C)C=C;
InChI	1S/C6H9B3O3/c1-4-7-10-8(5-2)12-9(6-3)11-7/h4-6H,1-3H2;
InChIKey	WBRSYBLNSTYNPP-UHFFFAOYSA-N
性质
化学式	C6H9B3O3
摩尔质量	161.57 g·mol−1
外观	无色液体
密度	0.89 g/ml
沸点	114 °C（387 K）
危险性
	GHS危险性符号;
GHS提示词	警告
H-术语	H302, H315, H319, H335
P-术语	P261, P264, P264+265, P270, P271, P280, P301+317, P302+352, P304+340, P305+351+338, P319, P321, P330, P332+317
主要危害	可溶
	若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。

三乙烯基环三硼氧烷是一种有机硼化合物，是环三硼氧烷（英语：Boroxine）的一种。

应用

三乙烯基环三硼氧烷可用于制备苯乙烯衍生物^[2]及乙烯酯。^[3]

^ Bower, John F.; Williams, Andrew J.; Woodward, Hannah L.; Szeto, Peter; Lawrence, Ron M.; Gallagher, Timothy. Reactivity of cyclic sulfamidates towards phosphonate-stabilised enolates: synthesis and applications of α-phosphono lactams. Organic & Biomolecular Chemistry. 2007, 5 (16): 2636–2644. PMID 18019539. doi:10.1039/B706315F.
^ Coleman, Claire M.; O'Shea, Donal F. New Organolithium Addition Methodology to Diversely Functionalized Indoles. Journal of the American Chemical Society. 1 April 2003, 125 (14): 4054–4055. PMID 12670219. doi:10.1021/ja034283h.
^ Staderini, Matteo; Gambardella, Alessia; Lilienkampf, Annamaria; Bradley, Mark. A Tetrazine-Labile Vinyl Ether Benzyloxycarbonyl Protecting Group (VeZ): An Orthogonal Tool for Solid-Phase Peptide Chemistry (PDF). Organic Letters. 1 June 2018, 20 (11): 3170–3173. PMID 29791161. doi:10.1021/acs.orglett.8b00898.