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2-((R)-4-Bromo-1,5-dimethyl-hex-4-enyl)-5-methyl-phenol is a complex organic compound characterized by its unique molecular structure. It features a phenol group, which is a hydroxyl group (-OH) attached to a benzene ring, and a 4-bromo-1,5-dimethyl-hex-4-enyl side chain, which includes a bromine atom, two methyl groups, and a double bond. The "R" configuration at the 4-position of the side chain indicates the specific arrangement of the atoms in space. 2-((R)-4-Bromo-1,5-dimethyl-hex-4-enyl)-5-methyl-phenol is likely to be used in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its structural diversity and potential reactivity. Its properties, such as solubility and reactivity, would be influenced by the presence of the bromine atom and the methyl groups, making it a potentially valuable intermediate in organic synthesis.

79399-41-0

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79399-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79399-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,9 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79399-41:
(7*7)+(6*9)+(5*3)+(4*9)+(3*9)+(2*4)+(1*1)=190
190 % 10 = 0
So 79399-41-0 is a valid CAS Registry Number.

79399-41-0Downstream Products

79399-41-0Relevant academic research and scientific papers

THE ABSOLUTE CONFIGURATION OF THE DICIPIENE DITERPENES

Croft, K. D.,Ghisalberti, E. L.,Jefferies, P. R.,Stuart, A. D.

, p. 383 - 387 (2007/10/02)

The absolute configuration of the dicipiene diterpenes has been determined by degradation to 4R-4-(2-methoxy-4-methylphenyl)-pentanoic acid.Photolysis of 1,18-diacetoxy-13-oxodecipi-14-ene proceeds through a novel photochemical reaction, formally a cycloreversion, to generate a key intermediate for the degradation.

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