65085-29-2 Usage
Structure
The compound contains a cyclohexadiene-1,4-dione structure, which is a six-membered ring with two double bonds and two ketone groups (C=O) on adjacent carbon atoms.
Decamethyltetracontadecaenyl moiety
The compound has a long aliphatic chain with 34 carbon atoms, which includes 10 double bonds (indicated by the numbers 3,7,11,15,19,23,27,31,35,39) and 10 methyl groups (indicated by the prefix "decamethyl").
Dimethoxy groups
The compound has two methoxy (-OCH3) groups attached to the cyclohexadiene-1,4-dione structure, which can influence its solubility and reactivity.
Methyl group
The compound also has a single methyl group (-CH3) attached to the cyclohexadiene-1,4-dione structure, further modifying its properties.
Stereochemistry
The compound has a specific stereochemistry, denoted by the Z,E,E,E,E,E,E,E,E designation. This indicates the relative positions of the substituents on the double bonds, with Z (from the German word "zusammen," meaning together) indicating that the two groups on the first double bond are on the same side, and E (from the German word "entgegen," meaning opposite) indicating that the groups on the subsequent double bonds are on opposite sides.
Unique chemical properties
Due to its complex structure and specific stereochemistry, the compound is likely to have unique chemical properties, such as reactivity, polarity, and solubility, which can be exploited in various applications.
Potential applications
The compound may have potential applications in fields such as pharmaceuticals, materials science, or organic synthesis, due to its unique structure and properties. Further research and experimentation would be needed to determine its specific uses and benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 65085-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,0,8 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65085-29:
(7*6)+(6*5)+(5*0)+(4*8)+(3*5)+(2*2)+(1*9)=132
132 % 10 = 2
So 65085-29-2 is a valid CAS Registry Number.
65085-29-2Relevant articles and documents
Highly S(N)2'-, (E)-, and antiselective alkylation of allylic phosphates. Facile synthesis of coenzyme Q10
Yanagisawa,Nomura,Noritake,Yamamoto
, p. 1130 - 1136 (2007/10/02)
Treatment of secondary allylic chlorides or allylic phosphates in tetrahydrofuran with prenyl Grignard reagent in the presence of CuCN · 2 LiCl gave geraniol or farnesol derivatives with high S(N)2' selectivity. Phosphate leaving groups were highly transstereoselective for the formation of (E,E)-farnesol derivatives. Furthermore, complete anti-S(N)2' selectivity was observed in the alkylation of optically active allylic phosphates. The present method appears to be an excellent carbon-carbon coupling reaction with high regio-, (E)-, and enantioselectivity. Coenzyme Q10 (ubiquinone 10) was efficiently synthesized using this methodology.
A Novel Solvent Effect in the Practical Synthesis of Ubiquinone-10
Eto, Hirozumi,Eguchi, Chikahiko
, p. 1597 - 1600 (2007/10/02)
The mixed solvent of nitromethane and hexane exhibited high stereoselectivity with good yields in the synthesis of ubiquinone-10 by the coupling of 2,3-dimethoxy-5-methylhydroquinone and isodecaprenol in the presence of a catalytic amount of BF3*OEt2.
REGIOSELECTIVE POLYPRENYL REARRANGEMENT OF POLYPRENYL 2,3,4,5-TETRASUBSTITUTED PHENYL ETHERS PROMOTED BY BORON TRIFLUORIDE
Yoshizawa, Toyokichi,Toyofuku, Hatsunori,Tachibana, Koichi,Kuroda, Toshio
, p. 1131 - 1134 (2007/10/02)
4-Acetoxy-6-polyprenyl-2,3,5-trimethylphenols or 2,3-dimethoxy-5-methyl-6-polyprenylhydroquinones were obtained selectively by the BF3*OEt2 catalyzed polyprenyl rearrangement of polyprenyl 4-acetoxy-2,3,5-trimethylphenyl ethers or polyprenyl 2,3-dimethoxy-4-hydroxy-5-methylphenyl ethers.
