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1-(3,5-di-tert-butyl-2-hydroxyphenyl)imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78009-23-1

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78009-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78009-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,0 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78009-23:
(7*7)+(6*8)+(5*0)+(4*0)+(3*9)+(2*2)+(1*3)=131
131 % 10 = 1
So 78009-23-1 is a valid CAS Registry Number.

78009-23-1Downstream Products

78009-23-1Relevant academic research and scientific papers

O -aryloxide-N-heterocyclic carbenes: Efficient synthesis of the proligands and their p -cymene ruthenium complexes

Yang, Dandan,Tang, Yungang,Song, Haibin,Wang, Baiquan

, p. 2012 - 2017 (2015)

An efficient method to synthesize o-hydroxyaryl-substituted imidazoles (2-OH-3-R-5-tBuC6H2)(C3H3N2) [R = tBu (1a), H (1b)] was developed through copper-catalyzed C-N bond formation. Treatment of 1a or 1b with a halohydrocarbon in refluxing toluene afforded a series of o-hydroxyaryl imidazolinium proligands 2a-h in high yields. Reactions of proligands 2a-h with Ag2O and [(p-cymene)RuCl2]2 gave the corresponding o-aryloxide-N-heterocyclic carbene ligated p-cymene ruthenium complexes 3a-h. All the imidazolium salts and ruthenium complexes were fully characterized by 1H and 13C NMR spectra, elemental analysis, and high-resolution mass spectrometry. Without the cocatalyst or irradiation, these complexes can efficiently catalyze norbornene ring-opening metathesis polymerization. Notably, the structures of the catalysts were found to have significant effects on the catalytic activity and the properties of obtained polymers.

CYCLOHEXADIENONES. 5. REACTION OF 4-HALO-2,4,6-TRI-t-BUTYL-2,5-CYCLOHEXADIEN-1-ONES WITH IMIDAZOLES

Fukata, Gouki,Itoh, Takashi,Tashiro, Masashi

, p. 549 - 554 (2007/10/02)

Reactions of 4-bromo- (1a) and 4-chloro-2,4,6-tri-t-butyl-2,5-cyclohexadien-1-one (1b) with imidazole (6b), 1-methyl- (6a), 2-methyl- (6c), 4-methylimidazole (6d), benzimidazole (6e), and 2-methylbenzimidazole (6f) was carried out under various conditions.It was found in these reactions that many products such as the 1-(4-oxo-2,5-cyclohexadienyl)-, 1-(2-hydroxyphenyl)- and 1-(4-hydroxyphenyl)imidazoles were formed and that the type of the products depended upon the structures of imidazoles 6.

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