597-52-4 | Triethylsilanol

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$26.00	$18.00
5g	98%	in stock	$42.00	$30.00
25g	98%	in stock	$110.00	$77.00
100g	98%	in stock	$387.00	$271.00

Description

• Catalog Number: AB80023
• Chemical Name: Triethylsilanol
• CAS Number: 597-52-4
• Molecular Formula: C6H16OSi
• Molecular Weight: 132.2761
• MDL Number: MFCD00042640
• SMILES: CC[Si](CC)(CC)O

Computed Properties

• Complexity: 51.3
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3

Literature

• Cyclodextrins selectively modified on both rims using an O-3-debenzylative post-functionalisation, a consequence of the Sorrento meeting.

  Carbohydrate research 20120715

• Total syntheses of ent-heliespirones A and C.

  The Journal of organic chemistry 20120106

• Ring cleavage reactions of methyl α-D-allopyranoside derivatives with phenylboron dichloride and triethylsilane.

  Molecules (Basel, Switzerland) 20111213

• Direct, one-pot reductive alkylation of anilines with functionalized acetals mediated by triethylsilane and TFA. Straightforward route for unsymmetrically substituted ethylenediamine.

  The Journal of organic chemistry 20110121

• Preparation of iron and gold silicide nanodomains on silicon (111) by the reaction of gold, iron-gold core-shell, and alloy nanoparticles with triethylsilane.

  ACS applied materials & interfaces 20100801

• Iridium-catalyzed (Z)-trialkylsilylation of terminal olefins.

  The Journal of organic chemistry 20100305

• Application of triethylsilane and palladium-charcoal-induced reductions in the synthesis of Fmoc-glutamic acid analogues.

  Advances in experimental medicine and biology 20090101

• Triethylsilane as a mild and efficient reducing agent for the preparation of alkanethiol-capped gold nanoparticles.

  Chemical communications (Cambridge, England) 20080907

• Solute-solvent complex kinetics and thermodynamics probed by 2D-IR vibrational echo chemical exchange spectroscopy.

  The journal of physical chemistry. B 20080821

• One-pot synthesis of oligosaccharides by combining reductive openings of benzylidene acetals and glycosylations.

  Organic letters 20080807

• (2+2) cycloaddition reaction of alkyl enol ethers with acrylates by in situ generated silyl triflic imide catalyst.

  Chemical & pharmaceutical bulletin 20080801

• Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols.

  Journal of the American Chemical Society 20080319

• Triethylsilanol: molecular conformations and role of the hydrogen-bonding oligomerization in its vibrational spectra.

  The journal of physical chemistry. A 20080221

• Pd-C-induced catalytic transfer hydrogenation with triethylsilane.

  The Journal of organic chemistry 20070817

• Nucleophilic aromatic substitution using Et3SiH/cat. t-Bu-P4 as a system for nucleophile activation.

  Chemical communications (Cambridge, England) 20070614

• Construction of fused bis(pyran) units from enones via a hydrosilylation-dihydroxylation-acetalization-reduction sequence.

  Chemical communications (Cambridge, England) 20061228

• Pd-catalyzed silicon hydride reductions of aromatic and aliphatic nitro groups.

  Organic letters 20051027

• Stereoselective synthesis of 4'-carbon-substituted xylofuranosyladenines.

  Nucleic acids symposium series (2004) 20040101