Lithium aluminum hydride solution [16853-85-3]

Cat# sc-228414A

Size : 1L

Marca : Santa Cruz Biotechnology

Contatta il distributore locale :


Telefono : +1 850 650 7790

Lithium aluminum hydride solution (CAS 16853-85-3)

0.0(0)
Écrire une critiquePoser une question

Application:
Lithium aluminum hydride solution is a reducing reagent
Numéro CAS:
16853-85-3
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

Informations pour la commande

Nom du produitRef. CatalogueCOND.Prix HTQTÉFavoris

Lithium aluminum hydride solution, 100 ml

sc-228414
100 ml
.00

Lithium aluminum hydride solution, 1 L

sc-228414A
1 L
.00
Lithium aluminum hydride solution is a reducing agent for asymmetric aldol reactions and synthesis of Li-Al-N-H composites.

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. 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
  3. Regeneration of lithium aluminum hydride.  |  Graetz, J., et al. 2008. J Am Chem Soc. 130: 17790-4. PMID: 19053465
  4. Reduction of venom alkaloids in Solenopsis richteriSolenopsis invicta hybrid: an attempt to identify new alkaloidal components.  |  Chen, L., et al. 2010. J Agric Food Chem. 58: 11534-42. PMID: 20964344
  5. Methylated polyamines as research tools.  |  Khomutov, AR., et al. 2011. Methods Mol Biol. 720: 449-61. PMID: 21318892
  6. Buckyball-, carbon nanotube-, graphite-, and graphene-enhanced dehydrogenation of lithium aluminum hydride.  |  Hsu, CP., et al. 2013. Chem Commun (Camb). 49: 8845-7. PMID: 23958824
  7. Investigation on the synthesis of 25-hydroxycholesterol.  |  Zhao, Q., et al. 2014. Steroids. 85: 1-5. PMID: 24582707
  8. Practical Synthesis of the Bicyclic Darunavir Side Chain: (3R,3aS,6aR)-Hexahydrofuro[2,3-b]furan-3-ol from Monopotassium Isocitrate.  |  Moore, GL., et al. 2017. Org Process Res Dev. 21: 98-106. PMID: 28539755
  9. Axially chiral hemiaminals from nonracemic alpha -amino acid derivatives (thiohydantoins): Synthesis and isomer identification.  |  Sarigul Ozbek, S. and Dogan, I. 2020. Chirality. 32: 1299-1310. PMID: 32770589
  10. Formaldehyde-free self-polymerization of lignin-derived monomers for synthesis of renewable phenolic resin.  |  Yang, W., et al. 2021. Int J Biol Macromol. 166: 1312-1319. PMID: 33161075
  11. Green synthesis of graphite from CO2 without graphitization process of amorphous carbon.  |  Liang, C., et al. 2021. Nat Commun. 12: 119. PMID: 33402678
  12. 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
  13. A new zeolitic lithium aluminum imidazolate framework.  |  Jiang, G., et al. 2021. Dalton Trans. 50: 7933-7937. PMID: 34075989
  14. General Method to Increase Carboxylic Acid Content on Nanodiamonds.  |  Shenoy, G., et al. 2022. Molecules. 27: PMID: 35164002
  15. 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