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1,4-Dihydro-1,4,5,6,8-pentamethyl-naphthalene is a polycyclic aromatic hydrocarbon with a molecular formula of C15H20. It is a derivative of naphthalene, where two hydrogen atoms are added to the molecule, and five methyl groups are attached to the carbon atoms at positions 1, 4, 5, 6, and 8. 1,4-dihydro-1,4,5,6,8-pentamethyl-naphthalene is characterized by its unique structure, which consists of two fused benzene rings with a saturated bridge between them. Due to its complex structure, it exhibits different chemical and physical properties compared to other naphthalene derivatives. It is primarily used as a research chemical and has potential applications in the synthesis of various organic compounds. However, it is important to note that, like other polycyclic aromatic hydrocarbons, it may have potential health risks and environmental concerns due to its carcinogenic properties.

2809-41-8

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2809-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2809-41-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2809-41:
(6*2)+(5*8)+(4*0)+(3*9)+(2*4)+(1*1)=88
88 % 10 = 8
So 2809-41-8 is a valid CAS Registry Number.

2809-41-8Upstream product

2809-41-8Downstream Products

2809-41-8Relevant academic research and scientific papers

Acetone condensation over sulfated zirconia catalysts

Al-Hazmi, Mohammed H.,Choi, Yongman,Apblett, Allen W.

, p. 705 - 716 (2013)

The aldol condensation reaction over sulfated zirconia led to the production of diacetone alcohol, which was further dehydrated forming mesityl oxide. The sulfated zirconia was obtained from zirconium acetate ethane sulfonate as a single source precursor. Oxides were obtained by calcinations of the precursors at 550-650 C, while the self-condensation reaction of acetone was carried out at 150 C. The precursor and the produced oxides were characterized using various characterization techniques. The precursors were synthesized with different acetate to ethane sulfonate ratio, ranging from 1 to 3. The major products obtained from the condensation reaction over the resulted oxide were mesityl oxide, mesitylene isophorone, naphthalene, and pentamers. The selectivity of mesityl oxide was approximately 100 % at the initial time-on-stream.

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