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Benzene, 1-(2-ethyl-1-butenyl)-2-ethynyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

819871-36-8

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819871-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 819871-36-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,9,8,7 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 819871-36:
(8*8)+(7*1)+(6*9)+(5*8)+(4*7)+(3*1)+(2*3)+(1*6)=208
208 % 10 = 8
So 819871-36-8 is a valid CAS Registry Number.

819871-36-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-ethylbut-1-enyl)-2-ethynylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,1-(2-ethyl-1-butenyl)-2-ethynyl

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:819871-36-8 SDS

819871-36-8Downstream Products

819871-36-8Relevant academic research and scientific papers

Gold-catalyzed cyclization/oxidative [3+2] cycloadditions of 1,5-enynes with nitrosobenzenes without additional oxidants

Chen, Chun-Hao,Tsai, Yen-Ching,Liu, Rai-Shung

supporting information, p. 4599 - 4603 (2013/05/21)

Golden control: The title reaction (see scheme) proceeds with high stereocontrol to generate the heterocyclic products in good yield. Experiments to probe the mechanism were performed. Copyright

Ruthenium-catalyzed cyclization of epoxide with a tethered alkyne: Formation of ketene intermediates via oxygen transfer from epoxides to terminal alkynes

Madhushaw, Reniguntala J.,Lin, Ming-Yuan,Abu Sohel, Shariar Md.,Liu, Rai-Shung

, p. 6895 - 6899 (2007/10/03)

Treatment of (o-ethynyl)phenyl epoxides with TpRuPPh3(CH 3CN)2PF6 (10 mol %) in hot toluene (100 °C, 3-6 h) gave 2-naphthols or 1-alkylidene-2-indanones very selectively with isolated yields exceeding 72%, depen

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