Triisopropylsilane

Triisopropylsilane
  • CAS No.:6485-79-6
Other grades of this product :
Triisopropylsilane Basic information
Product Name:Triisopropylsilane
Synonyms:Triisopropylsilane(L);Three isopropylsilane;Triisopropylsilane 99%;Triisopropylsilane Synonyms Triisopropylhydrosilane;HandyStep;PD-Tips;tris(propan-2-yl)silane;Triisopropylsilane, 98% 10GR
CAS:6485-79-6
MF:C9H22Si
MW:158.36
EINECS:464-880-1
Product Categories:Chemical Synthesis;Organometallic Reagents;Other Reagents;Reduction;Others;Synthetic Reagents;Si (Classes of Silicon Compounds);Si-H Compounds;Silicon Compounds (for Synthesis);Synthetic Organic Chemistry;Alkyl Silanes;Hydrogensilanes Hydrogensiloxanes;Reducing Agents;Biochemics;Organometallic Reagents;Organosilicon;OthersSynthetic Reagents;Silanes;bc0001
Mol File:6485-79-6.mol
Triisopropylsilane Chemical Properties
Boiling point 84-86 °C/35 mmHg (lit.)
density 0.773 g/mL at 25 °C (lit.)
refractive index n20/D 1.434(lit.)
Fp 99 °F
storage temp. Store below +30°C.
form liquid
Specific Gravity0.773
color colorless
Water Solubility Immiscible with water.
Sensitive Moisture Sensitive
Hydrolytic Sensitivity3: reacts with aqueous base
BRN 1733718
InChIKeyYDJXDYKQMRNUSA-UHFFFAOYSA-N
CAS DataBase Reference6485-79-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 10-36/37/38
Safety Statements 26-36-37/39-16
RIDADR UN 1993 3/PG 3
WGK Germany 3
10-21
TSCA No
HS Code 2931 90 00
HazardClass 3
PackingGroup III
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
Triisopropylsilane Usage And Synthesis
Chemical PropertiesClear colorless liquid
UsesThe bulky isopropyl groups (vs. ethyl) allow for more selective reductions, e.g., beta-selective reduction of anomeric C-phenyl ketals, but do not diminish their activity (e.g. in the copper triflate catalyzed reductive etherification of trimethylsilyl ethers).
UsesSelective silylation of primary hydroxy groups in the presence of secondary alcohol.
UsesTriisopropylsilane is used as a protecting group in peptide synthesis and is also used as a reducing agent for the selective reduction of anomeric C-phenyl ketals. It is used in the selective silylation of primary hydroxyl groups without affecting the secondary hydroxyl group. It is used in the preparation of anti-1,2-diols catalyzed by a Ni(O) N-heterocyclic carbine complex with high diastereoselectivity.
ApplicationVery sterically-hindered silane. Used as a cation scavenger in the deprotection of peptides.
Triisopropylsilane Preparation Products And Raw materials

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