6485-79-6 Triisopropylsilane CAS NO.6485-79-6
- FOB Price: USD: 300.00-300.00 /Kilogram Get Latest Price
- Min.Order: 1 Kilogram
- Payment Terms: L/C,T/T
- Available Specifications:
A(10-150)Kilogram
- Product Details
Keywords
- 6485-79-6 Triisopropylsilane
- 6485-79-6 Triisopropylsilane
- 6485-79-6 Triisopropylsilane
Quick Details
- ProName: 6485-79-6 Triisopropylsilane
- CasNo: 6485-79-6
- Molecular Formula: C9H22Si
- Appearance: Liquid
- Application: Organic Chemicals
- DeliveryTime: according to client's demand quantity
- PackAge: as requested
- Port: SHANGHAI
- ProductionCapacity: 100 Metric Ton/Day
- Purity: 99%
- Storage: room temperature
- Transportation: by sea
- LimitNum: 1 Kilogram
- Heavy metal: 10ppm
- Grade: Industrial Grade,Pharma Grade
- Transportation: LCL
Superiority
Product Name: Triisopropylsilane
Synonyms: 1.2.3-Triisopropyliden-cyclopropan;hexamethyl<3>radialene;TIPS-H;Triisopropyliden-cyclopropan;Triisopropylsilylhydride;Tris-isopropyliden-cyclopropan;Tris-isopropylsilane;(ME2CH)3SIH
CAS: 6485-79-6
MF: C9H22Si
MW: 158.36
EINECS: 464-880-1
Product Categories: Other Reagents;Reduction;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;Chemical Synthesis;Organometallic Reagents;Others;Synthetic Reagents
Mol File: 6485-79-6.mol
Triisopropylsilane Chemical Properties
Boiling point 84-86 °C35 mm Hg(lit.)
density 0.773 g/mL at 25 °C(lit.)
refractive index n20/D 1.434(lit.)
Fp 99 °F
storage temp. Store at RT.
form liquid
color colorless
Specific Gravity 0.773
Water Solubility Immiscible with water.
Hydrolytic Sensitivity 3: reacts with aqueous base
Sensitive Moisture Sensitive
BRN 1733718
InChIKey YDJXDYKQMRNUSA-UHFFFAOYSA-N
CAS DataBase Reference 6485-79-6(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
F 10-21
TSCA No
HS Code 2931 90 00
HazardClass 3
PackingGroup III
Triisopropylsilane Usage And Synthesis
Chemical Properties Clear colorless liquid
Uses The 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).
Uses Selective silylation of primary hydroxy groups in the presence of secondary alcohol.
Details
Product Name: Triisopropylsilane
Synonyms: 1.2.3-Triisopropyliden-cyclopropan;hexamethyl<3>radialene;TIPS-H;Triisopropyliden-cyclopropan;Triisopropylsilylhydride;Tris-isopropyliden-cyclopropan;Tris-isopropylsilane;(ME2CH)3SIH
CAS: 6485-79-6
MF: C9H22Si
MW: 158.36
EINECS: 464-880-1
Product Categories: Other Reagents;Reduction;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;Chemical Synthesis;Organometallic Reagents;Others;Synthetic Reagents
Mol File: 6485-79-6.mol
Triisopropylsilane Chemical Properties
Boiling point 84-86 °C35 mm Hg(lit.)
density 0.773 g/mL at 25 °C(lit.)
refractive index n20/D 1.434(lit.)
Fp 99 °F
storage temp. Store at RT.
form liquid
color colorless
Specific Gravity 0.773
Water Solubility Immiscible with water.
Hydrolytic Sensitivity 3: reacts with aqueous base
Sensitive Moisture Sensitive
BRN 1733718
InChIKey YDJXDYKQMRNUSA-UHFFFAOYSA-N
CAS DataBase Reference 6485-79-6(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
F 10-21
TSCA No
HS Code 2931 90 00
HazardClass 3
PackingGroup III
Triisopropylsilane Usage And Synthesis
Chemical Properties Clear colorless liquid
Uses The 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).
Uses Selective silylation of primary hydroxy groups in the presence of secondary alcohol.