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2,7-dimethylocta-1,7-diene-3,5-diyne is an organic compound with the molecular formula C10H12. It is a conjugated diene-diyne, which means it contains two carbon-carbon double bonds and two carbon-carbon triple bonds in its structure. The compound is characterized by the presence of two methyl groups attached to the second and seventh carbon atoms, respectively. This specific arrangement of functional groups and carbon atoms gives the molecule unique chemical properties and reactivity. It is an important building block in the synthesis of various organic compounds and can be used in the preparation of polymers, pharmaceuticals, and other specialty chemicals. Due to its complex structure, 2,7-dimethylocta-1,7-diene-3,5-diyne is a subject of interest in organic chemistry research, particularly in the study of conjugated systems and their applications.

5187-81-5

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5187-81-5 Usage

Type of compound

Alkyne
It contains at least one carbon-carbon triple bond.

Functional groups

Two methyl groups (CH3)
These are small alkyl groups attached to the main carbon chain.

Diene moiety

Two carbon-carbon double bonds separated by a single bond
This arrangement of double bonds contributes to the compound's reactivity and potential use in organic synthesis.

Reactivity

Reactive
The presence of triple and double bonds makes the compound more likely to undergo chemical reactions.

Utility

Valuable intermediate in organic synthesis
Due to its unique structure and reactivity, the compound can be used to produce various other organic compounds.

Potential applications

Production of other organic compounds
The compound can be used as a building block or intermediate in the synthesis of a wide range of organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 5187-81-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,8 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5187-81:
(6*5)+(5*1)+(4*8)+(3*7)+(2*8)+(1*1)=105
105 % 10 = 5
So 5187-81-5 is a valid CAS Registry Number.

5187-81-5SDS

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 2,7-dimethylocta-1,7-dien-3,5-diyne

1.2 Other means of identification

Product number -
Other names Diisopropenyldiacetylene

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:5187-81-5 SDS

5187-81-5Downstream Products

5187-81-5Relevant academic research and scientific papers

Ethynylbenzenoid metabolites of Antrodia camphorata: Synthesis and inhibition of TNF expression

Buccini, Marco,Punch, Kathryn A.,Kaskow, Belinda,Flematti, Gavin R.,Skelton, Brian W.,Abraham, Lawrence J.,Piggott, Matthew J.

, p. 1100 - 1113 (2014/02/14)

An improved synthesis of the anti-inflammatory natural product antrocamphin A (2), involving a key Castro-Stephens reaction, is presented, along with the first total synthesis of its congener antrocamphin B (3). Approaches towards the more complex co-meta

An alternative CuCl-piperidine-catalyzed oxidative homocoupling of terminal alkynes affording 1,3-diynes in air

Zheng, Qingwei,Hua, Ruimao,Wan, Youzhi

experimental part, p. 314 - 316 (2010/08/20)

CuCl with the use of a catalytic amount of piperidine as additive shows high catalytic activity for the oxidative homocoupling reactions of terminal alkynes in toluene at 60 ?C in air to afford 1,3-diynes in high yields. Copyright

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