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(2R,3R)-3-Hydroxy-2-methyl-2-propyl-cyclohexanone is a chiral organic compound with a cyclohexanone core structure. It is characterized by its specific stereochemistry, with the hydroxyl group (-OH) at the 3-position, a methyl group (-CH3) at the 2-position, and a propyl group (-C3H7) also at the 2-position. (2R,3R)-3-Hydroxy-2-methyl-2-propyl-cyclohexanone is a ketone, indicating the presence of a carbonyl group (C=O) between the 2- and 3-positions. The (2R,3R) notation specifies that both the 2- and 3-positions have the R (rectus) configuration, which refers to the arrangement of substituents in a specific three-dimensional orientation. (2R,3R)-3-Hydroxy-2-methyl-2-propyl-cyclohexanone is of interest in the field of organic chemistry, particularly in the synthesis of complex molecules and the study of stereochemistry.

90130-87-3

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90130-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90130-87-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,3 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90130-87:
(7*9)+(6*0)+(5*1)+(4*3)+(3*0)+(2*8)+(1*7)=103
103 % 10 = 3
So 90130-87-3 is a valid CAS Registry Number.

90130-87-3Downstream Products

90130-87-3Relevant academic research and scientific papers

Asymmetric Microbial Reduction of Prochiral 2,2-Disubstituted Cycloalkanediones

Brooks, Dee W.,Mazdiyasni, Hormoz,Grothaus, Paul G.

, p. 3223 - 3232 (2007/10/02)

Asymmetric microbial reduction of a series of 2,2-disubstituted 1,3-cycloalkanediones with bakers' yeast was examined as an example of an enzyme-catalyzed distinction of a substrate containing two trigonal carbonyl centers with stereoheterotropic faces an

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