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(1R,2S)-cis-di(methoxycarbonyloxy)cyclohexane is a chiral organic compound with a cyclohexane ring and two methoxycarbonyloxy groups attached to the 1st and 2nd carbon atoms in a cis configuration. (1R,2S)-cis-di(methoxycarbonyloxy)cyclohexane is characterized by its specific stereochemistry, where the R configuration is present at the 1st carbon and the S configuration at the 2nd carbon. The molecule is symmetrical due to the cis arrangement of the substituents, which are both on the same side of the cyclohexane ring. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, as its unique structure can be further modified to create a range of biologically active compounds.

58330-03-3

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58330-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58330-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,3 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58330-03:
(7*5)+(6*8)+(5*3)+(4*3)+(3*0)+(2*0)+(1*3)=113
113 % 10 = 3
So 58330-03-3 is a valid CAS Registry Number.

58330-03-3Downstream Products

58330-03-3Relevant academic research and scientific papers

Configurational Statistics of Poly(cyclohexene carbonate)

Yoshida, Naofumi,Aoki, Daisuke,Sasanuma, Yuji

, p. 9362 - 9374 (2020)

Conformational characteristics of poly(cyclohexene carbonate) (PCHC) have been investigated via molecular orbital (MO) calculations and NMR experiments on model compounds. The MO energies established through comparison with the NMR experiments were applied to the rotational isomeric state scheme with Bernoulli and Markov stochastic processes to yield configurational properties such as unperturbed characteristic ratio, its temperature coefficient, configurational entropy, tacticity entropy, and coherence number of PCHC chains including various stereosequences. trans-PCHC composed of (R,R)- and/or (S,S)-repeating units prefers a tg+t conformation in the O-CH-CH-O bond sequence of the (R,R)-unit, and its unperturbed characteristic ratio depends considerably on stereoregularity: isotactic, 29, and syndiotactic, 0.83 (in chloroform at 25 °C). cis-PCHC comprising (R,S)- and/or (S,R)-units exclusively adopts either g-g+g+ or g-g-g+ conformation in the O-CH-CH-O bond sequence of the (R,S)-unit partly owing to intramolecular hydrogen bonds, and the dependence of the characteristic ratio of cis-PCHC on stereoregularity would be completely opposite to that of trans-PCHC: isotactic, 0.59, and syndiotactic, 25. In terms of the abovementioned characteristic parameters, properties of PCHCs synthesized so far with stereospecific catalysts are discussed.

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