23056-94-2 Usage
Uses
Used in Pharmaceutical Industry:
2-METHYL-1-HEXEN-3-YNE is used as a chemical intermediate for the synthesis of pharmaceuticals. It plays a crucial role in the production of various medications, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical industry, 2-METHYL-1-HEXEN-3-YNE serves as a chemical intermediate for the synthesis of agrochemicals. It is utilized in the development of pesticides, herbicides, and other agricultural chemicals to improve crop yields and protect plants from pests.
Used in Organic Reactions:
2-METHYL-1-HEXEN-3-YNE is used as a reagent in organic reactions. Its unique chemical properties make it a valuable component in various chemical processes, facilitating the synthesis of complex organic molecules.
Used in Specialty Chemicals Production:
As a building block, 2-METHYL-1-HEXEN-3-YNE is used in the production of specialty chemicals. Its versatility allows it to be incorporated into a wide range of chemical products, enhancing their performance and functionality.
Safety Note:
It is important to handle and store 2-METHYL-1-HEXEN-3-YNE with care, as it is a flammable substance. Proper safety measures should be taken to prevent accidents and ensure the safe use of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 23056-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,5 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 23056-94:
(7*2)+(6*3)+(5*0)+(4*5)+(3*6)+(2*9)+(1*4)=92
92 % 10 = 2
So 23056-94-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H10/c1-4-5-6-7(2)3/h2,4H2,1,3H3
23056-94-2Relevant articles and documents
Gold-Catalyzed Rearrangement of Alkynyl Donor-Acceptor Cyclopropanes to Construct Highly Functionalized Alkylidenecyclopentenes
Chen, Huiyu,Zhang, Jing,Wang, David Zhigang
supporting information, p. 2098 - 2101 (2015/05/13)
A gold-catalyzed 1,7-addition-cyclization-elimination cascade sequence performed on a range of alkynyl-substituted donor-acceptor-type cyclopropanes provides facile entry to highly functionalized exo-alkylidenecyclopentenes under very mild conditions. Iso
Silver triflate-catalyzed cyclopropenation of internal alkynes with donor-/acceptor-substituted diazo compounds
Briones, John F.,Davies, Huw M. L.
supporting information; experimental part, p. 3984 - 3987 (2011/09/16)
Silver triflate was found to be an efficient catalyst for the cyclopropenation of internal alkynes using donor-/acceptor-substituted diazo compounds as carbenoid precursors. Highly substituted cyclopropenes, which cannot be synthesized directly via rhodium(II)-catalyzed carbenoid chemistry, can now be readily accessed.
Cu-catalyzed regioselective carbomagnesiation of dienes and enynes with sec- and tert-alkyl Grignard reagents
Todo, Hirohisa,Terao, Jun,Watanabe, Hideyuki,Kuniyasu, Hitoshi,Kambe, Nobuaki
, p. 1332 - 1334 (2008/12/21)
The carbomagnesiation of dienes and enynes with sec- and tert-alkyl Grignard reagents has been achieved by using copper salts as catalysts. The Royal Society of Chemistry.
