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5768-10-5

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5768-10-5 Usage

General Description

1,4-Bis(1-hydroxycyclohexyl)-1,3-butadiyne is a chemical compound with the molecular formula C14H20O2. It is a diacetylene derivative, which means it contains two adjacent triple bonds in its structure. 1,4-BIS(1-HYDROXYCYCLOHEXYL)-1,3-BUTADIYNE is used in the development of materials with specialized properties, such as photoresponsive polymers and liquid crystals. It is also used in the synthesis of functionalized carbon nanotubes. Due to its unique structure and properties, 1,4-Bis(1-hydroxycyclohexyl)-1,3-butadiyne has potential applications in a variety of fields, including materials science, nanotechnology, and drug delivery. However, it is important to handle this chemical with care due to its potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 5768-10-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,6 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5768-10:
(6*5)+(5*7)+(4*6)+(3*8)+(2*1)+(1*0)=115
115 % 10 = 5
So 5768-10-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H16N4S/c1-10-13(15-14(19)17-16-10)9-6-11-4-7-12(8-5-11)18(2)3/h4-9H,1-3H3,(H,15,17,19)

5768-10-5 Well-known Company Product Price

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  • Alfa Aesar

  • (L12492)  1,4-Bis(1-hydroxycyclohexyl)-1,3-butadiyne, 98+%   

  • 5768-10-5

  • 5g

  • 515.0CNY

  • Detail
  • Alfa Aesar

  • (L12492)  1,4-Bis(1-hydroxycyclohexyl)-1,3-butadiyne, 98+%   

  • 5768-10-5

  • 25g

  • 1971.0CNY

  • Detail

5768-10-5SDS

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 1-[4-(1-hydroxycyclohexyl)buta-1,3-diynyl]cyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names 1,1'-Butadiynylenedicyclohexanol

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:5768-10-5 SDS

5768-10-5Relevant articles and documents

Hay

, p. 3320 (1962)

Glycosyl Triazole Ligand for Temperature-Dependent Competitive Reactions of Cu-Catalyzed Sonogashira Coupling and Glaser Coupling

Mishra, Nidhi,Singh, Sumit K.,Singh, Anoop S.,Agrahari, Anand K.,Tiwari, Vinod K.

, p. 17884 - 17895 (2021/12/17)

Glycosyl triazoles have been introduced as efficient ligands for the Cu-catalyzed Sonogashira reaction to overcome the challenges of sideways homocoupling reactions in Cu catalysis in this reaction. The atmospheric oxygen in a sealed tube did not affect t

Facilitating Gold Redox Catalysis with Electrochemistry: An Efficient Chemical-Oxidant-Free Approach

Ye, Xiaohan,Zhao, Pengyi,Zhang, Shuyao,Zhang, Yanbin,Wang, Qilin,Shan, Chuan,Wojtas, Lukasz,Guo, Hao,Chen, Hao,Shi, Xiaodong

supporting information, p. 17226 - 17230 (2019/09/17)

Due to the high oxidation potential between AuI and AuIII, gold redox catalysis requires at least stoichiometric amounts of a strong oxidant. We herein report the first example of an electrochemical approach in promoting gold-catalyzed oxidative coupling of terminal alkynes. Oxidation of AuI to AuIII was successfully achieved through anode oxidation, which enabled facile access to either symmetrical or unsymmetrical conjugated diynes through homo-coupling or cross-coupling. This report extends the reaction scope of this transformation to substrates that are not compatible with strong chemical oxidants and potentiates the versatility of gold redox chemistry through the utilization of electrochemical oxidative conditions.

Ester functionalized hydrophobic task specific ionic liquid for Glaser coupling

Patil, Jayavant D.,Korade, Suyog N.,Chinchkar, Sarika M.,Pore, Dattaprasad M.

, p. 963 - 968 (2018/07/15)

A new hydrophobic ester functionalized task specific ionic liquid has been synthesized and its application explored in the synthesis of conjugated 1,3-diynes through Glaser coupling of terminal alkynes. Terminal alkynes undergo oxidativecoupling smoothly

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