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5,5-dimethyl-cyclohexane-1,3-diol is an organic compound with the molecular formula C8H16O2. It is a cyclic alcohol, specifically a diol, which means it contains two hydroxyl (-OH) groups. The compound features a cyclohexane ring, which is a six-carbon ring structure, with two methyl (-CH3) groups attached to the 5th carbon of the ring. The hydroxyl groups are located at the 1st and 3rd carbon positions of the ring. This chemical is known for its unique stereochemistry and can exist in various forms due to the different possible orientations of the hydroxyl groups. It is used in the synthesis of various organic compounds and can be found in the fragrance and flavor industry.

597-98-8

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597-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 597-98-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 597-98:
(5*5)+(4*9)+(3*7)+(2*9)+(1*8)=108
108 % 10 = 8
So 597-98-8 is a valid CAS Registry Number.

597-98-8Relevant academic research and scientific papers

Half-sandwich rhodium complexes with phenylene-based SCS ligands: Synthesis, characterization and catalytic activities for transfer hydrogenation of ketones

Jia, Wei-Guo,Gao, Li-Li,Zhi, Xue-Ting,Li, Xiao-Dong,Wang, Zhi-Bao,Sun, Ying

, (2021)

A series of half-sandwich rhodium complexes with tridentate phenylene-based bis(thione) (SCS) ligand have been synthesized and characterized. Both half-sandwich rhodium complexes and phenylene-based bis(thione) compounds were fully characterized by 1H and 13C NMR spectra, mass spectrometry and single-crystal X-ray diffraction method. The catalytic activities of half-sandwich rhodium complexes toward the transfer hydrogenation of ketones to their corresponding alcohols were explored using 2-propanol as hydrogen source and solvent. And the half-sandwich rhodium complexes exhibited high catalytic activity for transfer hydrogenation of ketones with a broad functional group tolerance.

Chemoselective formation of cyclo-aliphatic and cyclo-olefinic 1,3-diolsviapressure hydrogenation of potentially biobased platform molecules using Kn?lker-type catalysts

Alsters, Paul L.,Chou, Khi Chhay,De Wildeman, Stefaan M. A.,Faber, Teresa,Hadavi, Darya,Han, Peiliang,Quaedflieg, Peter J. L. M.,Schwalb Freire, Alfonso J.,Verzijl, Gerard K. M.,van Slagmaat, Christian A. M. R.

supporting information, p. 10102 - 10112 (2021/08/03)

The hydrogenative conversions of the biobased platform molecules 4-hydroxycyclopent-2-enone and cyclopentane-1,3-dione to their corresponding 1,3-diols are established using a pre-activated Kn?lker-type iron catalyst. The catalyst exhibits a high selectivity for ketone reduction, and does not induce dehydration. Moreover, by using different substituents of the ligand, thecis-transratio of the products can be affected substantially. A decent compatibility of this catalytic system with various structurally related substrates is demonstrated.

Rhodium coordination compound as well as preparation method and application thereof

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Paragraph 0139-0141, (2020/09/09)

The invention discloses a rhodium coordination compound as well as a preparation method and application thereof. The structure of the rhodium coordination compound is shown as a formula I which is described in the specification, wherein R is one of H and C1-C6 alkyl, and X is halogen. The rhodium coordination compound can efficiently catalyze a carbonyl transfer hydrogenation reaction to obtain corresponding alcohol, and meanwhile, the preparation method has the advantages of simple process and simplicity and convenience in operation.

Metal complexes with an adamantane-like structure

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, (2008/06/13)

PCT No. PCT/EP97/05206 Sec. 371 Date Apr. 14, 1999 Sec. 102(e) Date Apr. 14, 1999 PCT Filed Sep. 23, 1997 PCT Pub. No. WO98/16534 PCT Pub. Date Apr. 23, 1998In metal complexes of the formula I the substituents have the following meanings: M is a metal of

CYCLOALKANOL ESTERS OF DIHYDROLYSERGIC ACID USEFUL AS 5HT2 RECEPTOR ANTAGONISTS

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, (2008/06/13)

Cycloalkyl or ketocycloalkyl esters of 1-substituted-6-C 1-4 straight chain alkyl (or allyl)-ergoline-8β-carboxylic acids, useful as 5HT. sub.2 receptor antagonists.

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