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(1R,2S)-1-Methoxymethyl-2-vinyl-cyclohexanecarbaldehyde is a complex organic compound with the molecular formula C11H18O2. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific 1R,2S configuration. (1R,2S)-1-Methoxymethyl-2-vinyl-cyclohexanecarbaldehyde features a cyclohexane ring, which is a six-carbon ring structure, with a vinyl group (C=C) attached to the second carbon and a methoxymethyl group (-OCH3) attached to the first carbon. The aldehyde functional group (-CHO) is present, indicating that it has a carbonyl group with a hydrogen atom attached to it. (1R,2S)-1-Methoxymethyl-2-vinyl-cyclohexanecarbaldehyde is known for its unique scent and is used in the fragrance industry to create natural-smelling aromas. It is also used in the synthesis of various pharmaceuticals and other organic compounds due to its versatile structure.

81453-05-6

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81453-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81453-05-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,5 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 81453-05:
(7*8)+(6*1)+(5*4)+(4*5)+(3*3)+(2*0)+(1*5)=116
116 % 10 = 6
So 81453-05-6 is a valid CAS Registry Number.

81453-05-6Downstream Products

81453-05-6Relevant articles and documents

DIASTEREOSELECTIVE AND ENANTIOSELECTIVE SYNTHESIS OF 1,2-DISUBSTITUTED CYCLOALKANECARBOXALDEHYDES

Kogen, Hiroshi,Tomioka, Kiyoshi,Hashimoto, Shun-ichi,Koga, Kenji

, p. 3951 - 3956 (2007/10/02)

A highly useful method for diastereoselective and enantioselective synthesis of trans- and cis-1,2-disubstituted cycloalkanecarboxaldehydes (trans- and cis-10), useful chiral synthons having asymmetric tertiary and quaternary carbon atoms in vicinal positions in their rings, is devised starting from cycloalkenecarboxaldehydes (5). t-Leucine t-butyl ester (2.R=But), a highly effective chiral auxiliary reagent in the present method, can be recovered for recycling without any loss of optical purity.Some mechanistic explanations on the strereochemical courses of the reactions are presented.

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