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Undec-1,5-diyne is an organic compound with the molecular formula C11H16. It is a conjugated diene, which means it has two carbon-carbon triple bonds separated by a single carbon-carbon single bond. This unique structure gives it interesting chemical properties and potential applications in various fields, such as polymer chemistry and materials science. The compound is also known for its ability to undergo various chemical reactions, including cycloadditions and rearrangements, making it a valuable building block in synthetic chemistry.

10160-98-2

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10160-98-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10160-98-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,6 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10160-98:
(7*1)+(6*0)+(5*1)+(4*6)+(3*0)+(2*9)+(1*8)=62
62 % 10 = 2
So 10160-98-2 is a valid CAS Registry Number.

10160-98-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name undeca-1,5-diyne

1.2 Other means of identification

Product number -
Other names 1,5-undecadiyne

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:10160-98-2 SDS

10160-98-2Relevant academic research and scientific papers

A new method for the preparation of 1,5-diynes. Synthesis of (4E,6Z,10Z)-4,6,10-hexadecatrien-1-ol, the pheromone component of the cocoa pod borer moth Conopomorpha cramerella

Pereira, Alban R.,Cabezas, Jorge A.

, p. 2594 - 2597 (2005)

(Figure Presented) A new method for the synthesis of 1,5-diynes, from the reaction of 1,3-dilithiopropyne and propargyl chlorides, was developed. This new methodology was used to prepare (4E,6Z,10Z)-4,6,10-hexadecatrien-1-ol, one of the pheromone componen

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