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triethyl(octyl)silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10175-53-8 Structure
  • Basic information

    1. Product Name: triethyl(octyl)silane
    2. Synonyms: silane, triethyloctyl-; Triethyl(octyl)silane
    3. CAS NO:10175-53-8
    4. Molecular Formula: C14H32Si
    5. Molecular Weight: 228.4894
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10175-53-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 261.964°C at 760 mmHg
    3. Flash Point: 97.885°C
    4. Appearance: N/A
    5. Density: 0.774g/cm3
    6. Vapor Pressure: 0.018mmHg at 25°C
    7. Refractive Index: 1.426
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: triethyl(octyl)silane(CAS DataBase Reference)
    11. NIST Chemistry Reference: triethyl(octyl)silane(10175-53-8)
    12. EPA Substance Registry System: triethyl(octyl)silane(10175-53-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 10175-53-8(Hazardous Substances Data)

10175-53-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10175-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,7 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10175-53:
(7*1)+(6*0)+(5*1)+(4*7)+(3*5)+(2*5)+(1*3)=68
68 % 10 = 8
So 10175-53-8 is a valid CAS Registry Number.

10175-53-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name triethyl(octyl)silane

1.2 Other means of identification

Product number -
Other names et3Si(n-oct)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10175-53-8 SDS

10175-53-8Downstream Products

10175-53-8Relevant articles and documents

Phosphoramidite complexes of Pd(II), Pt(II) and Rh(I): An effective hydrosilylation catalyst of 1-hexyne and 1-octene

Carroll, Hannah K.,Parlane, Fraser G.L.,Reich, Noah,Jelier, Benson J.,Montgomery, Craig D.

, p. 78 - 83 (2017/06/13)

The hydrophosphorane HP(OC6H4NMe)2 was used to prepare the diastereotopic complexes [MCl2{P(OC6H4NMe)OC6H4NHMe}] (M?=?Pd, Pt) by reaction with [MCl2(PhCN)2], and [RhCl(PPh3){P(OC6H4NMe)OC6H4NHMe}] by reaction with [RhCl(PPh3)3]. To form these complexes, the phosphorane undergoes ring-opening, whereby it is coordinated as the tautomeric neutral phosphoramidite-amino chelating ligand. The crystal structure of [RhCl(PPh3){P(OC6H4NMe)OC6H4NHMe}] was determined and the geometry about the Rh(I) atom is square-planar with cis-disposed phosphorus-donor ligands. The Rh–P distance is shortened (2.1056(6) ?) due to Rh(d)?→?P π-backbonding. In addition, [RhCl(PPh3){P(OC6H4NMe)OC6H4NHMe}] was shown to be an effective regio- and stereoselective catalyst for the hydrosilylation of 1-octene and 1-hexyne.

Effect of triarylphosphane ligands on the rhodium-catalyzed hydrosilylation of alkene

Xue, Mei,Li, Jiayun,Peng, Jiajian,Bai, Ying,Zhang, Guodong,Xiao, Wenjun,Lai, Guoqiao

, p. 120 - 126 (2014/02/14)

A series of triarylphosphanes (1a, 2a, 3a, 4a, 5a, 6a, 7a, 8a, 9a, 10a, 11a) have been synthesized. An X-ray crystal structure analysis of (2-bromophenyl)diphenylphosphane (1a) unambiguously confirmed the constitution of the functionalized phosphane. The hydrosilylation reaction of styrene with triethoxysilane catalyzed with RhCl3/triarylphosphane was studied. In comparison with the classic Wilkinson's catalyst, rhodium complexes with functionalized triarylphosphane ligands are characterized by a very high catalytic effectiveness for the hydrosilylation of alkene. Among these catalysts tested, RhCl3/diphenyl(2-(trimethylsilyl)phenyl)phosphane (8a) exhibited excellent catalytic properties. Using this silicon-containing phosphane ligand for the rhodium-catalyzed hydrosilylation of styrene, both higher conversion of alkene and higher β-adduct selectivity were obtained than with Wilkinson's catalyst.

Highly selective dehydrogenative silylation of alkenes catalyzed by rhenium complexes

Jiang, Yanfeng,Blacque, Olivier,Fox, Thomas,Freeh, Christian M.,Berke, Heinz

experimental part, p. 2121 - 2128 (2009/09/30)

Rhenium(I) complexes of type [ReBr2(L)(NO)(PR3) 2] (L = H2 (1), CH3CN (2), and ethylene (3); R = iPr (a) and cyclohexyl (Cy; b)) catalyze dehydrogenative silylation of alkenes in a highly selective ma

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