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5,7-Dodecadiyne-1,12-diol is a chemical compound with the molecular formula C12H20O2. It is a diol, meaning it contains two hydroxyl (-OH) functional groups, and it also contains a triple bond between carbon atoms.

74602-32-7

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74602-32-7 Usage

Uses

Used in Organic Synthesis:
5,7-Dodecadiyne-1,12-diol is used as a building block in organic synthesis for the production of various organic compounds and materials. Its unique structure with a triple bond and two hydroxyl groups allows for versatile chemical reactions and the creation of a wide range of products.
Used in Pharmaceutical Development:
5,7-Dodecadiyne-1,12-diol is used as a key intermediate in the development of new pharmaceuticals. Its functional groups and structural features make it a valuable component in the synthesis of drug candidates, potentially leading to the discovery of novel therapeutic agents.
Used in Research as a Reagent:
5,7-Dodecadiyne-1,12-diol serves as a reagent in chemical research, enabling scientists to study various chemical reactions and mechanisms. Its presence in experiments can provide insights into the behavior of different functional groups and their interactions with other molecules.
Used in Pharmaceutical Industry:
5,7-Dodecadiyne-1,12-diol is used as a chemical intermediate for the synthesis of pharmaceutical compounds. Its unique structure contributes to the development of new drugs with potential therapeutic benefits.
Used in Materials Science:
5,7-Dodecadiyne-1,12-diol is used as a component in the design and synthesis of new materials with specific properties. Its incorporation into materials can lead to advancements in areas such as polymer science, nanotechnology, and material engineering.
Used in Chemical Manufacturing:
5,7-Dodecadiyne-1,12-diol is utilized in the chemical manufacturing industry as a raw material for the production of various chemical products. Its versatility and reactivity make it a valuable asset in the synthesis of a wide range of compounds used in different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 74602-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,0 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74602-32:
(7*7)+(6*4)+(5*6)+(4*0)+(3*2)+(2*3)+(1*2)=117
117 % 10 = 7
So 74602-32-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O2/c13-11-9-7-5-3-1-2-4-6-8-10-12-14/h13-14H,5-12H2

74602-32-7 Well-known Company Product Price

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  • Alfa Aesar

  • (L11485)  5,7-Dodecadiyne-1,12-diol, 96%   

  • 74602-32-7

  • 1g

  • 416.0CNY

  • Detail
  • Alfa Aesar

  • (L11485)  5,7-Dodecadiyne-1,12-diol, 96%   

  • 74602-32-7

  • 5g

  • 1603.0CNY

  • Detail

74602-32-7SDS

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 5,7-Dodecadiyne-1,12-Diol

1.2 Other means of identification

Product number -
Other names dodeca-5,7-diyne-1,12-diol

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:74602-32-7 SDS

74602-32-7Relevant academic research and scientific papers

Synthesis and Evaluation of a Series of Bis(pentylpyridinium) Compounds as Antifungal Agents

Obando, Daniel,Koda, Yasuko,Pantarat, Namfon,Lev, Sophie,Zuo, Xiaoming,Bijosono Oei, Johanes,Widmer, Fred,Djordjevic, Julianne T.,Sorrell, Tania C.,Jolliffe, Katrina A.

supporting information, p. 1421 - 1436 (2018/07/29)

A series of bis(4-pentylpyridinium) compounds with a variety of spacers between the pyridinium headgroups was synthesised, and the antifungal activity of these compounds was investigated. Lengthening the alkyl spacer between the pentylpyridinium headgroups from 12 to 16 methylene units resulted in increased antifungal activity against C. neoformans and C. albicans, but also resulted in increased hemolytic activity and cytotoxicity against mammalian cells. However, inclusion of an ortho-substituted benzene ring in the centre of the alkyl spacer resulted in decreased cytotoxicity and hemolytic activity, while maintaining antifungal potency. Replacement of the alkyl and aromatic-containing spacers by more hydrophilic ethylene glycol groups resulted in a loss of antifungal activity. Some of the compounds inhibited fungal PLB1 activity, but the low correlation of this inhibition with antifungal potency indicates PLB1 inhibition is unlikely to be the predominant mode of antifungal action of this class of compounds, with preliminary studies suggesting they may act via disruption of fungal mitochondrial function.

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