15869-93-9 Usage
Description
3,5-DIMETHYLOCTANE, also known as an alkane with methyl groups substituted at positions 3 and 5, is a metabolite observed in cancer metabolism. It is a hydrocarbon compound with a specific structure that makes it of interest in various applications.
Uses
Used in Chemical Industry:
3,5-DIMETHYLOCTANE is used as a chemical intermediate for the synthesis of various organic compounds. Its unique structure allows it to be a valuable building block in the creation of different molecules, particularly in the pharmaceutical and agrochemical industries.
Used in Fuel Industry:
3,5-DIMETHYLOCTANE is used as a component in the formulation of high-quality fuels. Its properties contribute to improved combustion efficiency and reduced emissions, making it a desirable additive in the fuel industry.
Used in Research and Development:
3,5-DIMETHYLOCTANE serves as a valuable research tool in the study of cancer metabolism. Its presence in cancer cells can provide insights into the metabolic pathways and mechanisms involved in the development and progression of cancer, potentially leading to the discovery of novel therapeutic targets and strategies.
Used in Environmental Applications:
3,5-DIMETHYLOCTANE can be utilized in the development of advanced materials for environmental remediation, such as adsorbents for the removal of pollutants from air, water, and soil. Its unique chemical properties make it suitable for these applications, contributing to a cleaner and healthier environment.
Check Digit Verification of cas no
The CAS Registry Mumber 15869-93-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,6 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15869-93:
(7*1)+(6*5)+(5*8)+(4*6)+(3*9)+(2*9)+(1*3)=149
149 % 10 = 9
So 15869-93-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H22/c1-5-7-10(4)8-9(3)6-2/h9-10H,5-8H2,1-4H3
15869-93-9Relevant articles and documents
Synthesis of mesoporous ZSM-5 zeolites and catalytic cracking of ethanol and oleic acid into light olefins
Zhao, Tingting,Li, Fuwei,Yu, Hongchang,Ding, Shilei,Li, Zhixia,Huang, Xinyuan,Li, Xiang,Wei, Xiaohan,Wang, Zhenlin,Lin, Hongfei
, p. 101 - 110 (2019/02/24)
Conversion of biomass-derived chemicals into light olefins is a promising method to maintain sustainable development of light olefin industry. In this study, three mesoporous ZSM-5 zeolites (MZSM-5-A, MZSM-5-B and MZSM-5-C) with major pore diameter about 4.8 nm, 16 nm and 22 nm were synthesized using a hydrothermal method by utilizing different templates. The catalytic activity of catalysts was studied by catalytic cracking of ethanol and oleic acid. The influence of reaction temperature on conversion and product selectivity was investigated. The characterization of ZSM-5 samples showed that the orders of the external surface area and mesopore volume were MZSM-5-C > MZSM-5-B > MZSM-5-A > conventional HZSM-5. In ethanol to light olefin reaction, MZSM-5-C achieved the highest light olefin yield (318.3 mL g?1) and ethylene selectivity (42.3%) at 400 °C. In oleic acid to light olefin reaction, MZSM-5-B achieved a complete conversion of oleic acid at 500 °C, and obtained the highest light olefin selectivity (38.1%) at 550 °C. The difference may be relevant to the size and chemical structure of feedstock molecular as well as the acidity of catalysts. Regardless of ethanol or oleic acid as feedstock, introduction of mesopore in zeolites significantly enhanced the light olefin yield and selectivity.
ORGANOBORON COMPOUNDS. 398. CONDENSATION OF TRIALLYLBORON WITH ALKENYLACETYLENES
Mikhailov, B. M.,Bubnov, Yu. N.,Frolov, S. I.
, p. 1736 - 1741 (2007/10/02)
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