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Silane, triethyl(1-methylenepentyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42067-74-3

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42067-74-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42067-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,6 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42067-74:
(7*4)+(6*2)+(5*0)+(4*6)+(3*7)+(2*7)+(1*4)=103
103 % 10 = 3
So 42067-74-3 is a valid CAS Registry Number.

42067-74-3SDS

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 2-(triethylsilyl)-1-hexene

1.2 Other means of identification

Product number -
Other names 2-Triethylsilyl-1-hexen

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:42067-74-3 SDS

42067-74-3Downstream Products

42067-74-3Relevant academic research and scientific papers

Catalytic hydrosilylation of acetylenes mediated by phosphine complexes of cobalt(I), rhodium(I), and iridium(I)

Field, Leslie D.,Ward, Antony J.

, p. 91 - 97 (2003)

The complexes [Co(PPh3)3Cl] (1), [Co(PPh3)2(CO)2Cl] (2), [Co(PMe3)3Cl] (3), [Co(PMe3)2(CO)2Cl] (4), [Rh(dppe)(CO)Cl] (5), [Rh(PPh2Me)2(CO)Cl] (6), [Ir(dppe)(CO)Br] (7), and [Ir(PPh2Me)2 (CO)Cl] (8) catalyse the hydrosilylation of a range of acetylenes including 1-hexyne, phenylacetylene, and 1-phenyl-1-propyne with triethylsilane. In the case of 1-hexyne and 1-phenyl-1-propyne, only the expected hydrosilylation products were observed; however, when the substrate was phenylacetylene, cyclotrimerisation and dimerisation products were observed in addition to the expected vinylsilanes. No hydrosilation was observed with alkene substrates; however, in the presence of some metal complexes, there was double bond migration and cis/trans-isomerisation probably mediated by the formation of metal hydrides in the reaction mixture.

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