沸点	346 ºC
闪点	163 ºC
密度	1.291

没有数据	没有数据

来源	SDS样本
没有数据	没有数据

产品合成路线

更多

名称	CAS号

更多

文章

同行评议文献

[The reduction of prostaglandin intermediate with diisobutylaluminium hydride].Z Y Liu et al.Yao xue xue bao = Acta pharmaceutica Sinica, 17(4), 296-298 (1982-04-01) Diisobutylaluminum hydride mediated regioselective O desilylations: access to multisubstituted cyclodextrins.Ramprasad Ghosh et al.Angewandte Chemie (International ed. in English), 51(7), 1548-1552 (2011-10-19) Macromolecular engineering of polyactones and polyactides. 12. Study of the depolymerization reactions of poly (. epsilon.-caprolactone) with functional aluminum alkoxide end groups.Dubois P, et al. Macromolecules, 26(17), 4407-4412 (1993) Use of multivariate statistical techniques to optimize the separation of 17 capsinoids by ultra performance liquid chromatography using different columns.Janclei P Coutinho et al.Talanta, 134, 256-263 (2015-01-27) Regioselective ring opening of benzylidene acetal protecting group(s) of hexopyranoside derivatives by DIBAL-H.Nobuo Tanaka et al.Carbohydrate research, 343(15), 2675-2679 (2008-08-23) Lactone-free ginkgolides via regioselective DIBAL-H reduction.Hideki Ishii et al.Organic & biomolecular chemistry, 3(19), 3471-3472 (2005-09-21) Synthesis of enantiopure non-natural alpha-amino acids using tert-butyl (2S)-2-[bis-(tert-butoxycarbonyl)amino]-5-oxopentanoate as key-intermediate:the first synthesis of(S)-2-amino-oleic acid.V Constantinou-Kokotou et al.The journal of peptide research : official journal of the American Peptide Society, 58(4), 325-331 (2001-10-19) Synthesis of peptide macrocycles using unprotected amino aldehydes.Rotstein BH, et al. Nature Protocols, 5(11), 1813-1813 (2010) Triisobutylaluminium and diisobutylaluminium hydride as molecular scalpels: the regioselective stripping of perbenzylated sugars and cyclodextrins.Thomas Lecourt et al.Chemistry (Weinheim an der Bergstrasse, Germany), 10(12), 2960-2971 (2004-06-24) Reversible cyclopropane ring-cleavage reactions within etheno-bridged [4.3.1]propelladiene frameworks leading to aza- and oxa-[5.6.5.6]fenestratetraenes.Nora Heinrich et al.Chemistry (Weinheim an der Bergstrasse, Germany), 18(43), 13585-13588 (2012-09-19) Reduction of tertiary phosphine oxides with DIBAL-H.Carl A Busacca et al.The Journal of organic chemistry, 73(4), 1524-1531 (2008-01-17) Regioselective synthesis of heterocycles containing nitrogen neighboring an aromatic ring by reductive ring expansion using diisobutylaluminum hydride and studies on the reaction mechanism.Hidetsura Cho et al.The Journal of organic chemistry, 75(3), 627-636 (2009-12-31) A direct entry to substituted N-methoxyamines from N-methoxyamides via N-oxyiminium ions.Kenji Shirokane et al.Angewandte Chemie (International ed. in English), 49(36), 6369-6372 (2010-07-31) Substitution effect of purine nucleosides on diisobutylaluminum hybride reduction.K Hirota et al.Nucleic acids symposium series, (34)(34), 15-16 (1995-01-01) DIBAL-mediated reductive transformation of trans-dimethyl tartrate acetonide into ε-hydroxy α,β-unsaturated ester and its derivatives.Takashi Tomioka et al.The Journal of organic chemistry, 76(11), 4669-4674 (2011-04-30) Oxabicyclo[3.2.1]octenes in organic synthesis: direct ring opening of oxabicyclo[3.2.1] ring systems with diisobutylaluminum hydride and a silyl ketene acetal--synthesis of the chiral C(19)-C(26) and C(27)-C(32) fragments of Scytophycin C.Kevin W Hunt et al.Organic letters, 4(2), 245-248 (2002-02-14) Diisobutylaluminum hydride reductions revitalized: a fast, robust, and selective continuous flow system for aldehyde synthesis.Damien Webb et al.Organic letters, 14(2), 568-571 (2011-12-31) Improved procedure for the reductive acetylation of acyclic esters and a new synthesis of ethers.D J Kopecky et al.The Journal of organic chemistry, 65(1), 191-198 (2000-05-18) DIBALH mediated reduction of the acetal moiety on perhydrofuro[2,3-b]pyran derivatives.J Marco-Contelles et al.Carbohydrate research, 335(1), 63-70 (2001-09-13) Facile reductive cleavage of purine nucleosides to acyclonucleosides using diisobutylaluminium hydride (DIBAL): a new synthetic method for the preparation of 9-ribitylpurine derivatives.Y Kitade et al.Nucleic acids symposium series, (27)(27), 107-108 (1992-01-01) [Development of domino reactions based on skeletal rearrangement].Kenji Sugimoto Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 131(11), 1563-1573 (2011-11-02)

备注