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2-Propenoic acid, 3-(triethylsilyl)-, ethyl ester, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104014-91-7

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104014-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104014-91-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,1 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 104014-91:
(8*1)+(7*0)+(6*4)+(5*0)+(4*1)+(3*4)+(2*9)+(1*1)=67
67 % 10 = 7
So 104014-91-7 is a valid CAS Registry Number.

104014-91-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-carbethoxy-2-(triethylsilyl)ethylene

1.2 Other means of identification

Product number -
Other names ethyl (E)-3-(triethylsilyl)propenoate

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:104014-91-7 SDS

104014-91-7Downstream Products

104014-91-7Relevant academic research and scientific papers

Single-Operation Synthesis of Vinylsilanes from Alkenes and Hydrosilanes with the Aid of Ru3(CO)12

Seki, Yoshio,Takeshita, Kenji,Kawamoto, Kazuaki,Murai, Shinji,Sonoda, Noboru

, p. 3890 - 3895 (1986)

Alkenes (RCH=CH2, where R = C6H5, p-CH3C6H4, p-CH3OC6H4, p-ClC6H4, 2-naphthyl, (CH3)3C, Me3SiO(CH3)2C, n-C4H9O, and Et3Si) with HSiEt3 with Ru3(CO)12 as a catalyst gave corresponding vinylsilanes (1, 6-13) without formation of simple addition products.Hydrosilanes such as HSiMe3, HSiEt2Me, HSiPhMe2, and HSi(OEt)3 also yielded vinylsilanes.Alkenes having a hydrogen atom at the allylic position (1-hexene, allylbenzene, 3-phenoxyprop-1-ene, vinylcyclohexane, β-methylstyrene, α-methylstyrene, 2-hexene) formed mixtures of vinylsilanes and allylsilanes.The ratio of vinylsilane 16 to allylsilane 17 decreased with an increase in temperature and with time.Substituted styrenes with a hydrosilane in the presence of 1-hexene gave vinylsilanes 1 and 6-8 in good yields based on the styrenes along with n-hexane.

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