Lithium aluminum hydride [16853-85-3]

Referencia sc-215254

embalaje : 10g

Marca : Santa Cruz Biotechnology

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Lithium aluminum hydride (CAS 16853-85-3)

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Noms alternatifs:
Lithium tetrahydridoaluminate; LAH; Lithium alanate; Lithium tetrahydroaluminate
Application:
Lithium aluminum hydride is a powerful reagent and reducing agent
Numéro CAS:
16853-85-3
Pureté:
≥95%
Masse Moléculaire:
37.95
Formule Moléculaire:
LiAlH4
Information supplémentaire:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
Pour la Recherche Uniquement. Non conforme pour le Diagnostic ou pour une Utilisation Thérapeutique.
Available in US only.
* Consulter le Certificat d'Analyses pour les données spécifiques à un lot (incluant la teneur en eau).

ACCÈS RAPIDE AUX LIENS

Lithium aluminum hydride can be used as a reactant or a reagent for a variety of experiments. For instance, it has been used for the preparation of thermoplastic polyester polyamides from oleic acid, Lithium-polymer batteries, hydrodefluorination of gem-difluoromethylene derivatives, asymmetric aldol reactions and synthesis of Li-Al-N-H composites with hydrogen absorption/ desorption properties. Additionally, Lithium aluminum hydride is a powerful reducing agent for many different reduction reactions such as that of ketones to alcohols.

References:

  1. Stereospecific reduction of phosphine oxides to phosphines by the use of a methylation reagent and lithium aluminum hydride.  |  Imamoto, T., et al. 2001. Org Lett. 3: 87-90. PMID: 11429879
  2. Reaction of lithium aluminum hydride with elemental selenium: its application as a selenating reagent into organic molecules.  |  Ishihara, H., et al. 2001. J Am Chem Soc. 123: 8408-9. PMID: 11516295
  3. A theoretical study of the reaction of lithium aluminum hydride with formaldehyde and cyclohexanone.  |  Luibrand, RT., et al. 2001. J Org Chem. 66: 7254-62. PMID: 11681935
  4. Some generalizations relative to lithium aluminum hydride reactions.  |  GAYLORD, NG. 1954. Experientia. 10: 350-6. PMID: 13200500
  5. Electrometric titration of volatile oils and volatile oil isolates using lithium aluminum hydride.  |  LINTNER, CJ., et al. 1950. J Am Pharm Assoc Am Pharm Assoc. 39: 415-7. PMID: 15428385
  6. Regeneration of lithium aluminum hydride.  |  Graetz, J., et al. 2008. J Am Chem Soc. 130: 17790-4. PMID: 19053465
  7. Reduction of prion infectivity and levels of scrapie prion protein by lithium aluminum hydride: implications for RNA in prion diseases.  |  Jeong, BH., et al. 2009. J Neuropathol Exp Neurol. 68: 870-9. PMID: 19606066
  8. Methylated polyamines as research tools.  |  Khomutov, AR., et al. 2011. Methods Mol Biol. 720: 449-61. PMID: 21318892
  9. Green synthesis of graphite from CO2 without graphitization process of amorphous carbon.  |  Liang, C., et al. 2021. Nat Commun. 12: 119. PMID: 33402678
  10. In-beam Mössbauer spectra of 57Mn implanted into lithium aluminum hydride.  |  Sato, Y., et al. 2021. Appl Radiat Isot. 170: 109582. PMID: 33561749
  11. Nucleophilic transformations of azido-containing carbonyl compounds via protection of the azido group.  |  Aimi, T., et al. 2021. Chem Commun (Camb). 57: 6062-6065. PMID: 34036976
  12. A new zeolitic lithium aluminum imidazolate framework.  |  Jiang, G., et al. 2021. Dalton Trans. 50: 7933-7937. PMID: 34075989
  13. General Method to Increase Carboxylic Acid Content on Nanodiamonds.  |  Shenoy, G., et al. 2022. Molecules. 27: PMID: 35164002
  14. Inverse Electron-Demand Aza-Diels-Alder Reaction of alpha , beta -Unsaturated Thioesters with In Situ-Generated 1,2-Diaza-1,3-dienes for the Synthesis of 1,3,4-Thiadiazines.  |  Shen, LW., et al. 2022. J Org Chem. 87: 4232-4240. PMID: 35212520
  15. Determination of neutral manufacturing impurities in heroin by capillary gas chromatography with electron capture detection after reduction with lithium aluminum hydride and derivatization with heptafluorobutyric anhydride.  |  Moore, JM., et al. 1986. Anal Chem. 58: 1003-7. PMID: 3717563

Informations pour la commande

Nom du produitRef. CatalogueCOND.Prix HTQTÉFavoris

Lithium aluminum hydride, 10 g

sc-215254
10 g
.00

Lithium aluminum hydride, 25 g

sc-215254A
25 g
.00