922-59-8 Usage
Uses
Used in Organic Synthesis:
3-METHYL-1-PENTYNE is employed as a key intermediate in organic synthesis, serving as a building block for the creation of more complex organic molecules. Its unique structure allows for versatile reactions and the formation of a diverse range of compounds.
Used in Pharmaceutical Production:
3-METHYL-1-PENTYNE is used as a starting material or intermediate in the synthesis of various pharmaceuticals. Its reactivity and structural properties make it valuable in the development of new drugs and medications.
Used in Agrochemical Production:
3-METHYL-1-PENTYNE also finds application in the agrochemical industry, where it is used in the synthesis of pesticides, herbicides, and other agricultural chemicals. Its role in these processes contributes to the development of effective and targeted products for crop protection.
Used as a Solvent:
Due to its properties, 3-METHYL-1-PENTYNE can be used as a solvent in certain chemical reactions. Its ability to dissolve a variety of substances makes it a useful component in certain industrial processes.
Used as a Reagent:
In various chemical reactions, 3-METHYL-1-PENTYNE is utilized as a reagent, facilitating specific transformations and reactions that are essential in the synthesis of target compounds.
It is crucial to handle 3-METHYL-1-PENTYNE with care due to its highly flammable nature and potential for violent reactions with oxidizing agents, ensuring safety in its application across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 922-59-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 922-59:
(5*9)+(4*2)+(3*2)+(2*5)+(1*9)=78
78 % 10 = 8
So 922-59-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H10/c1-4-6(3)5-2/h1,6H,5H2,2-3H3
922-59-8Relevant academic research and scientific papers
MAIN GROUP METAL CHEMISTRY. REACTION OF 3,3-DIALKYL-1-BROMOALLENES WITH ALUMINIUM, ZINC, AND MAGNESIUM REAGENTS
Caporusso, Anna Maria,Lardicci, Luciano,Settimo, Federico da
, p. 599 - 602 (2007/10/02)
The reactions between 1-bromo-3-methyl-1,2-pentadiene and isobutyl compounds of main group metals (Al, Zn, Mg) provide reduction, elimination, and alkylation products with chemo- and regioselectivity depending on the nature of the organometallic reagent.
Untersuchungen zur Kinetik und zum Mechanismus der Addition von Methylradikalen an Vinylacetylen
Scherzer, K.,Claus, P.,Karwath, M.
, p. 321 - 328 (2007/10/02)
The addition of methyl radicals to vinylacetylen has been studied at 573 K.The methyl radicals were produced by thermolysis of azomethane.The attack occurs exclusively in the terminal positions and predominantly at the triple bond.The value of the rate constant amounts to k2.1 + k2.2 = 5.1E6 l mol-1s-1.The main steps and the formed types of radicals are deduced from the stable products.Without azomethane vinylacetylene is consumed by a slow conversion of second order.The activation parameters of this dimerisation were estimated at 553-593 K.
