| Chemical Name | Diisobutylaluminium hydride |
| CAS Number | 1191-15-7 |
| EC Number | 214-729-9 |
| Beilstein Registry Number | 4123663 |
| MDL Number | MFCD00008928 |
| Synonym |
氫化二異丁基鋁
DIBAL-H
Al-Alchili
二异丁基氢化铝, 25%甲苯溶液
Aluminum, diisobutylhydro-
DIISOBUTYLALUMINUM HYDRIDE
Bis(isobutyl)hydroaluminum
二异丁基氢化铝, 20% (CA 1M) SOLN. IN TOLUENE
氢化二异丁基铝
hydrobis(2-methylpropyl)-aluminu
hydrobis(2-methylpropyl)-Aluminum
DIBAL-H;DIBAL
Aluminum, hydrodiisobutyl-
DIISOBUTYLALUMINIUM HYDRIDE
Aluminum, hydrobis(2-methylpropyl)-
DIBAH
二异丁基氢化铝 溶液
Diisobutylhydroaluminum
DIBAL-H DIBAL
hydrobis(2-methylpropyl)aluminum
二异丁基氢化铝
DI-I-BUTYLALUMINUM HYDRIDE
Diisobutylaluminum
二异丁基氢化铝, 1M SOLUTION IN HEXANE |
| PubChem Substance ID | 24852856 |
| Chemical Name Translation | 二异丁基氢化铝 |
| Wiswesser Line Notation | 1Y1&1-AL-H1Y1&1 |
| IUPAC Name | bis(2-methylpropyl)alumane |
⑴.无色液体,高度易燃。引起严重灼伤。吞食可能造成肺部损伤。蒸汽可能引起困倦和眩晕。
⑵.主要用作精细化学品的还原剂和氢铝化剂。
⑶.具有强烈的吸湿性,对空气和湿气敏感,遇水会发生激烈反应放出氢气。
⑷.四氢呋喃不适宜作溶剂,因为两者反应生成配位化合物。二异丁基氢化铝是一种新型金属有机化合物,可使酮、羧酸、酯选择性还原成相应的醛或者醇。
Used in Pd-catalyzed reductive debromination of secondary alkyl bromides. O-Debenzylation and ring opening of perbenzylated furanosides. Convenient in situ generation of HZrCp2Cl from ZrCp2Cl2 and DIBAL-H.
{PUB} Crystallography Open Database (COD)|PubChem --- Diisobutylaluminum Hydride Promoted Cyclization of o-(Trimethylsilylethynyl)styrenes to Indenes --- https://pubmed.ncbi.nlm.nih.gov/25093271
{ALD} Merck: 14,10425
{ALD} Merck: 14,10425 Beilstein:4(4)4400
{PUB} Nature Chemistry|PubChem|Springer Nature --- Enantioselective radical C–H amination for the synthesis of β-amino alcohols --- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7390680
{PUB} Nature Chemistry|PubChem|Springer Nature --- Quaternary stereocentres via catalytic enantioconvergent nucleophilic substitution reactions of tertiary alkyl halides --- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7925339
{PUB} Nature Chemistry|Springer Nature --- A ring expansion strategy towards diverse azaheterocycles --- https://pubmed.ncbi.nlm.nih.gov/34282307
{PUB} Nature Chemistry|Springer Nature --- Polymerization of silanes through dehydrogenative Si–Si bond formation on metal surfaces --- https://pubmed.ncbi.nlm.nih.gov/33782562
{PUB} PubChem --- A Direct Entry to Substituted N‐Methoxyamines from N‐Methoxyamides via N‐Oxyiminium Ions --- https://pubmed.ncbi.nlm.nih.gov/20672260
{PUB} PubChem --- A rapid and efficient one-pot method for the reduction of N-protected α-amino acids to chiral α-amino aldehydes using CDI/DIBAL-H --- https://pubmed.ncbi.nlm.nih.gov/26421937
{PUB} PubChem --- Alkylation of Pyridines at Their 4‐Positions with Styrenes plus Yttrium Reagent or Benzyl Grignard Reagents --- https://pubmed.ncbi.nlm.nih.gov/25352343
{PUB} PubChem --- Regioselective ring opening of benzylidene acetal protecting group(s) of hexopyranoside derivatives by DIBAL-H --- https://pubmed.ncbi.nlm.nih.gov/18718576
{PUB} PubChem --- Substitution effect of purine nucleosides on diisobutylaluminum hybride reduction --- https://pubmed.ncbi.nlm.nih.gov/8841529
{PUB} PubChem --- Synthesis of Prenyl‐ and Geranyl‐Substituted Carbazole Alkaloids by DIBAL‐H Promoted Reductive Pyran Ring Opening of Dialkylpyrano[3,2‐a]carbaz