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Cyclodecyne, also known as decacyclene, is a cyclic alkyne with the molecular formula C10H10. It is a member of the cycloalkyne family, characterized by its ten carbon atoms arranged in a closed ring structure. Cyclodecyne is an interesting molecule due to its unique electronic properties and potential applications in materials science and organic chemistry. It is synthesized through various methods, including the coupling of appropriate precursors and the use of transition metal catalysts. The molecule exhibits interesting reactivity, such as its ability to undergo Diels-Alder reactions and other cycloadditions, making it a subject of interest for researchers exploring new synthetic pathways and materials.

3022-41-1

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3022-41-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3022-41-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,2 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3022-41:
(6*3)+(5*0)+(4*2)+(3*2)+(2*4)+(1*1)=41
41 % 10 = 1
So 3022-41-1 is a valid CAS Registry Number.

3022-41-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclodecyne

1.2 Other means of identification

Product number -
Other names Cyclodecyne

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:3022-41-1 SDS

3022-41-1Relevant academic research and scientific papers

Generation of hexahydroazulenes

Kr?mer, Guido,Detert, Heiner,Meier, Herbert

body text, p. 4810 - 4812 (2009/10/26)

(Z)-Cyclodec-1-en-6-yne (3) generates three conjugated hexahydroazulenes 3→1k→1c, 1? under FVP conditions, whereas flash vacuum pyrolysis (FVP) of cyclodecyne (2) leads to 1,2,9-decatriene (9). We attribute the different thermal behavior of 2 (ring opening) and 3 (ring closure) to different transannular interactions. Altogether 22 constitutional isomers of hexahydroazulene should exist; three new isomers (1k, 1?, and 1m) are presented here, ten were described earlier, but the reinvestigation of the dehydration route of bicyclic alcohol 11 showed that one of the ten structures has to be revised.

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