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(1S,4S)-4-Hydroxymethyl-3,5,5-trimethyl-cyclohex-2-enol, also known as (1S,4S)-3,5,5-trimethyl-4-(hydroxymethyl)cyclohex-2-en-1-ol, is a chiral organic compound with a molecular formula of C10H18O2. It features a cyclohexane ring with a double bond at the 2-position, three methyl groups at the 3, 5, and 5 positions, and a hydroxymethyl group at the 4-position. (1S,4S)-4-Hydroxymethyl-3,5,5-trimethyl-cyclohex-2-enol is an enantiomer, with the specific configuration of the hydroxyl and methyl groups at the 1 and 4 positions being in the S configuration. It is a colorless liquid with a molecular weight of 170.25 g/mol. (1S,4S)-4-Hydroxymethyl-3,5,5-trimethyl-cyclohex-2-enol is of interest in organic chemistry and may have potential applications in the synthesis of various pharmaceuticals and natural products due to its unique structure and chirality.

76739-77-0

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76739-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76739-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,7,3 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76739-77:
(7*7)+(6*6)+(5*7)+(4*3)+(3*9)+(2*7)+(1*7)=180
180 % 10 = 0
So 76739-77-0 is a valid CAS Registry Number.

76739-77-0Upstream product

76739-77-0Relevant academic research and scientific papers

153. Synthese von optisch aktiven, natuerlichen Carotinoiden und strukturell verwandten Naturprodukten. IV. Synthese von (3R,3'R,6'R)-Lutein

Mayer, Hans,Ruettimann, August

, p. 1451 - 1455 (2007/10/02)

The synthesis of (3R,3'R,6'R)-lutein (19) according to the building principle C25+C15=C40 is reported utilizing (R)-4-hydroxy-2,6,6-trimethyl-2-cyclohexen-1-one (4) as a readily available key intermediate.

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