产品名称

英文名称：Dibutylboryl trifluoromethanesulfonate solution

同义词

60669-69-4、Dibutylboron trifluoromethanesulfonate、dibutylboranyl trifluoromethanesulfonate、DIBUTYLBORYL TRIFLUOROMETHANESULFONATE、Dibutylboron triflate、Dibutyl(((trifluoromethyl)sulfonyl)oxy)borane、Dibutylboron triflate; Dibutylboron trifluoromethanesulfo、二丁基硼三氟甲磺酸盐 溶液

产品性质

CAS编号：60669-69-4

分子式：C9H18BF3O3S

分子量：274.11

PubChem编号：2724243

别名：二丁基硼三氟甲磺酸盐 溶液

英文别名：60669-69-4|Dibutylboron trifluoromethanesulfonate|dibutylboranyl trifluoromethanesulfonate|DIBUTYLBORYL TRIFLUOROMETHANESULFONATE|Dibutylboron triflate|Dibutyl(((trifluoromethyl)sulfonyl)oxy)borane|Dibutylboron triflate; Dibutylboron trifluoromethanesulfo

规格或纯度：0.7mol/L in diethyl ether,Energyseal

英文名称：Dibutylboryl trifluoromethanesulfonate solution

储存温度：室温

运输条件：常规运输

备注：卖完停产，不再备货

产品介绍：Dibutylboryl trifluoromethanesulfonate (Dibutylboron triflate, Bu2BOTf) is an organometallic reagent. It efficiently promotes the1,4-addition of benzylic and allylic organocopper reagents.Dibutylboryl trifluoromethanesulfonate (Dibutylboron triflate, Bu2BOTf) may be used in the following studies ? Stereo- and regio-selective synthesis of erythro aldols. ? As promoter for the solution and polymer-supported trichloroacetimidate-based glycosylations. ? Synthesis of β-alkoxy carbonyl compounds, via one-step Mukaiyama aldol-type reaction. ? Aldol-type cyclization for the stereoselective synthesis of cyclic ethers. ? As reagent for the formation of boron enolates. ? As a complexation aid for the isolation of 1-acyldipyrromethanes.Dibutylboryl trifluoromethanesulfonate (Dibutylboron triflate, Bu2BOTf) is an organometallic reagent. It efficiently promotes the1,4-addition of benzylic and allylic organocopper reagents.Dibutylboryl trifluoromethanesulfonate (Dibutylboron triflate, Bu2BOTf) may be used in the following studies ? Stereo- and regio-selective synthesis of erythro aldols. ? As promoter for the solution and polymer-supported trichloroacetimidate-based glycosylations. ? Synthesis of β-alkoxy carbonyl compounds, via one-step Mukaiyama aldol-type reaction. ? Aldol-type cyclization for the stereoselective synthesis of cyclic ethers. ? As reagent for the formation of boron enolates. ? As a complexation aid for the isolation of 1-acyldipyrromethanes.

IUPAC Name：dibutylboranyl trifluoromethanesulfonate

INCHI：InChI=1S/C9H18BF3O3S/c1-3-5-7-10(8-6-4-2)16-17(14,15)9(11,12)13/h3-8H2,1-2H3

InChi Key：FAVAVMFXAKZTMV-UHFFFAOYSA-N

Canonical SMILES：B(CCCC)(CCCC)OS(=O)(=O)C(F)(F)F

Isomeric SMILES：B(CCCC)(CCCC)OS(=O)(=O)C(F)(F)F

PubChem CID：2724243

象形图：

信号词：Danger

危险声明：H314 Causes severe skin burns and eye damageH318 Causes serious eye damage

预防措施声明：P280,P321,P405,P501,P264,P260,P301+P330+P331,P304+P340,P363,P264+P265,P305+P354+P338,P317,P302+P361+P354,P316

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