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2-METHYL-1-OCTEN-3-YNE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17603-76-8

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17603-76-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17603-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,0 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17603-76:
(7*1)+(6*7)+(5*6)+(4*0)+(3*3)+(2*7)+(1*6)=108
108 % 10 = 8
So 17603-76-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H14/c1-4-5-6-7-8-9(2)3/h2,4-6H2,1,3H3

17603-76-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyloct-1-en-3-yne

1.2 Other means of identification

Product number -
Other names 2-Methyl-1-octene-3-yne

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:17603-76-8 SDS

17603-76-8Relevant academic research and scientific papers

Copper-catalyzed silylation reactions of propargyl epoxides: Easy access to 2,3-allenols and stereodefined alkenes

Chang, Xi-Hao,Liu, Zheng-Li,Luo, Yun-Cheng,Yang, Chao,Liu, Xiao-Wei,Da, Bing-Chao,Li, Jie-Jun,Ahmad, Tanveer,Loh, Teck-Peng,Xu, Yun-He

supporting information, p. 9344 - 9347 (2017/08/23)

Efficient silylation reactions of propargyl epoxides catalyzed by copper catalysts have been developed. Under mild reaction conditions, tri- and tetra-substituted functionalized allenols and alkenes could be selectively obtained in moderate to high yields

Beyond the limits: Palladium-N-heterocyclic carbene-based catalytic system enables highly efficient [4+2] benzannulation reactions

Zatolochnaya, Olga V.,Galenko, Alexey V.,Gevorgyan, Vladimir

supporting information; experimental part, p. 1149 - 1155 (2012/06/16)

A highly efficient catalytic system for the palladium-catalyzed [4+2] benzannulation reaction of enynes and enynophiles has been developed. The use of an N-heterocyclic carbene-based palladium precursor allowed us to achieve turnover numbers up to 1800. T

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