41044-63-7 Usage
Uses
Used in Organic Synthesis:
(5E)-2-Methyl-1,5-heptadiene is used as an intermediate in the chemical industry for the synthesis of various organic chemicals. Its carbon-carbon double bonds make it a versatile building block for creating a range of compounds with diverse applications.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, (5E)-2-Methyl-1,5-heptadiene serves as an intermediate in the production of different medications. Its reactivity and structural features allow for the development of new drugs with potential therapeutic benefits.
Used in Fragrance Industry:
(5E)-2-Methyl-1,5-heptadiene is also utilized as a fragrance ingredient in the perfume and cosmetics industry. Its unique scent profile contributes to the creation of various fragrances used in personal care products.
Used in Cosmetics Industry:
In the cosmetics industry, (5E)-2-Methyl-1,5-heptadiene is employed for its scent properties, enhancing the sensory experience of various cosmetic products and making them more appealing to consumers.
Safety Precautions:
Given its flammability and potential health risks, (5E)-2-Methyl-1,5-heptadiene should be handled with care. Appropriate safety measures, including the use of personal protective equipment and proper storage conditions, are essential to minimize the risk of fire and exposure to this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 41044-63-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,4 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41044-63:
(7*4)+(6*1)+(5*0)+(4*4)+(3*4)+(2*6)+(1*3)=77
77 % 10 = 7
So 41044-63-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H14/c1-4-5-6-7-8(2)3/h4-5H,2,6-7H2,1,3H3/b5-4+
41044-63-7Relevant academic research and scientific papers
The Thermolysis of 2,2-Dimethyl-1-vinylcyclobutane
Chickos, James S.,Frey, H. Monty
, p. 365 - 370 (2007/10/02)
The kinetics of thermolysis of 2,2-dimethyl-1-vinylcyclobutane have been investigated as a function of temperature from 263 to 301 deg C.Primary products produced in the reaction include isobutene and butadiene, 4,4-dimethylcyclohexene, 2-methylhepta-1,6-diene, and cis-2-methylhepta-1,5-diene. trans-2-Methylhepta-1,5-diene and 2,4-dimethylhexa-1,5-diene are produced from cis-2-methylhepta-1,5-diene by way of a 3,3-sigmatropic rearrangement.The reaction obeys first-order kinetics and is unaffected by surface.Activation energies (kcal mol-1) and (logA/s-1) for the overall decomposition and for formation of the primary products are 45.73 +/- 0.3 (14.427 +/- 0.12), 47.71 +/- 0.7 (15.087 +/- 0.3), 44.35 +/- 1.6 (12.53 +/- 0.6), 45.0 +/-1.3 (12.24 +/- 0.5), and 38.38 +/- 1.7 (10.785 +/- 0.7), respectively.The regiochemistry observed in fragmentation and in the 1,3-sigmatropic rearrangement of the starting material is discussed in terms of substituent effects found in other cyclobutane and vinylcyclobutane thermolyses.The fragmentation process and the isomerization to 4,4-dimethylcyclohexene and 2-methylhepta-1,6-diene is believed to proceed through the intervention of 6-methylhept-1-ene-3,6-diyl. cis-2-Methylhepta-1,5-diene is formed from a concerted 1,5-sigmatropic rearrangement of the starting material.The factors which affect the stereochemistry of the 1,5-hydrogen shift are discussed.
