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2-(5-decynyloxy)tetrahydro-2H-pyran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51652-45-0

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51652-45-0 Usage

Class

Alkynyl ethers

Structure

Tetrahydro-2H-pyran ring and a decynyl group

Usage

Building block in organic synthesis, reagent in chemical reactions, production of pharmaceuticals, agrochemicals, and industrial products

Potential biological activities

Anti-cancer and anti-microbial agent

Versatility

Diverse potential applications in chemistry and medicine

Check Digit Verification of cas no

The CAS Registry Mumber 51652-45-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,5 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51652-45:
(7*5)+(6*1)+(5*6)+(4*5)+(3*2)+(2*4)+(1*5)=110
110 % 10 = 0
So 51652-45-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O2/c1-2-3-4-5-6-7-8-10-13-16-15-12-9-11-14-17-15/h15H,2-4,7-14H2,1H3

51652-45-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-dec-5-ynoxyoxane

1.2 Other means of identification

Product number -
Other names EINECS 257-337-3

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:51652-45-0 SDS

51652-45-0Relevant academic research and scientific papers

Chemistry of natural compounds and bioorganic chemistry a convergent synthesis of octadeca-2E,13Z-dienyl acetate, a pheromone component of Synanthedon tipuliformis C

Ishmuratov,Yakovleva,Kharisov,Kunafina,Gorobets,Kuchin,Tolstikov

, p. 1465 - 1467 (2007/10/03)

A convergent synthesis of octadeca-2E,13Z-dienyl acetate, a pheromone component of Synanthedon tipuliformis C., has been developed. The synthesis is based on cross-coupling of 8-iodooct-2E-en-1-ol THP ether with dec-57-enyl bromide catalyzed by CuBr.

A Tandem Synthesis of (+/-)-Euphococcinine and (+/-)-Adaline

Davison, Edwin C.,Holmes, Andrew B.,Forbes, Ian T.

, p. 9047 - 9050 (2007/10/02)

Intramolecular hydroxylamine-alkyne cyclisation of the hydroxylamines 8 and 9 afforded six-membered cyclic nitrones which without isolation underwent a tandem intramolecular dipolar cycloaddition to produce the tricyclic isoxazolidines 6 and 7 respectively.These were converted in two steps into the ladybird defence alkaloids (+/-)-euphococcinine 4 and (+/-)-adaline 5.

SYNTHESIS OF HIGHER ACETYLENIC ALCOHOLS

Kovalev, B. G.,Matveeva, E. D.,Stan, V. V.,Vovk, G. A.,Yudin, L. G.,Kost, A. N.

, p. 1728 - 1733 (2007/10/02)

The alkylation of 1-alkynes in various solvents was investigated, and the optimum conditions for the production of acetylenic alcohols were obtained.

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