51065-64-6 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
6-Methyl-2-heptyne is used as a key building block in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the creation of a wide range of compounds with potential therapeutic and pesticidal properties.
Used as a Solvent:
Due to its chemical properties, 6-Methyl-2-heptyne serves as a solvent in certain industrial applications, facilitating the dissolution and interaction of various substances.
Used in Dye and Pigment Manufacturing:
6-Methyl-2-heptyne is utilized in the production of dyes and pigments, contributing to the development of vibrant colors and stable compounds for use in various industries.
Used in Automotive and Aerospace Industries:
6-Methyl-2-heptyne finds applications in the automotive and aerospace sectors as a fuel additive, enhancing the performance and efficiency of fuels. It is also a component in the formulation of lubricants and corrosion inhibitors, ensuring the longevity and reliability of machinery and equipment.
Safety Precautions:
Given its reactive nature, 6-Methyl-2-heptyne should be handled with care and stored in a cool, well-ventilated area away from sources of heat and ignition to prevent accidents and ensure safe usage.
Check Digit Verification of cas no
The CAS Registry Mumber 51065-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,6 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51065-64:
(7*5)+(6*1)+(5*0)+(4*6)+(3*5)+(2*6)+(1*4)=96
96 % 10 = 6
So 51065-64-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H14/c1-4-5-6-7-8(2)3/h8H,6-7H2,1-3H3
51065-64-6Relevant academic research and scientific papers
On 1.2-Shift Reactions and C-H-Insertions of Acyclic Alkylidene Carbenes
Ondruschka, Bernd,Remmler, Matthias,Zimmermann, Gerhard,Krueger, Christian
, p. 49 - 54 (2007/10/02)
Two series of acyclic terminal vinyl bromides (1...4 and 5...7) were tested in the reaction with potassium tert-butoxide as precursors of alkylidene carbenes.As expected 1 up to 4 only give 1-alkynes whereas the 2-methylated vinyl bromides 5, 6 and 7 yield 1-methylated cyclopentenes predominantly besides 2-alkynes.The formation of cyclopentenes indicates a reaction route via alkylidene carbenes and 1,5-C-H-insertion reactions, that of 2-alkynes is convincing evidence for 1,2-alkyl shift reactions in 2-methyl substituted alkylidene carbenes.The selectivity of 1,5-C-H-insertion depends on the degree of alkyl substitution of the C-5-atom.At 240 deg C the selectivity is 1deg:2deg:3deg ca. 1:54:240.
