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The chemical compound "(1R)-2t.4c-dibromo-1r-methyl-4t-isopropyl-cyclohexanone-(3)" is a complex organic molecule with a cyclohexanone ring structure. It is characterized by the presence of two bromine atoms, a methyl group, and an isopropyl group. The compound is a chiral molecule, indicated by the "1R" notation, which specifies the configuration of the chiral center at the first carbon atom. The "2t" and "4c" descriptors refer to the trans and cis configurations of the substituents at the second and fourth carbon atoms, respectively. The "1r" and "4t" notations further specify the relative positions of the methyl and isopropyl groups. (1R)-2t.4c-dibromo-1r-methyl-4t-isopropyl-cyclohexanone-(3) is likely to have unique physical and chemical properties due to its specific stereochemistry and functional groups.

43205-85-2

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43205-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 43205-85-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,2,0 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 43205-85:
(7*4)+(6*3)+(5*2)+(4*0)+(3*5)+(2*8)+(1*5)=92
92 % 10 = 2
So 43205-85-2 is a valid CAS Registry Number.

43205-85-2Upstream product

43205-85-2Relevant academic research and scientific papers

Stereoselective synthesis of (6R)- and (6S)-diosphenol and Ψ-diosphenol

Schneider, David F,Viljoen, Murray S

, p. 5307 - 5315 (2007/10/03)

Methods are discussed for the stereoselective synthesis of the (R)-and (S)-enantiomers of the diosphenols (5)-(8) by utilizing the commercially available stereoisomers (9), (12), (23) and (25) of carvone and limonene, respectively, as chiral starting materials.

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