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D.l-trans-2-ethoxycarbonylamino-cyclohexanol-(1) is a complex organic compound with the molecular formula C10H19NO3. It is a chiral molecule, meaning it has a non-superimposable mirror image, and the "d.l" prefix indicates that it is a racemic mixture, containing both the dextrorotatory (d) and levorotatory (l) enantiomers. d.l-trans-2-Aethoxycarbonylamino-cyclohexanol-(1) features a cyclohexanol ring, which is a six-carbon cyclic structure with a hydroxyl group, and an ethoxycarbonylamino group attached to the second carbon. The ethoxycarbonyl group is an ester derivative of carbamic acid, providing a protective group for the amino function. d.l-trans-2-Aethoxycarbonylamino-cyclohexanol-(1) is significant in organic synthesis, particularly in the preparation of amino acids and their derivatives, and may have applications in pharmaceuticals and chemical research due to its unique structural features.

2955-77-3

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2955-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2955-77-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,5 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2955-77:
(6*2)+(5*9)+(4*5)+(3*5)+(2*7)+(1*7)=113
113 % 10 = 3
So 2955-77-3 is a valid CAS Registry Number.

2955-77-3Relevant academic research and scientific papers

CAN (ETHOXYCARBONYL)NITRENE SELECTIVITY BE CONTROLLED BY MICELLAR PSEUDOPHASE?

Bertolaccini, Riccardo,Cerichelli, Giorgio,Loreto, M. Antonietta,Pellacani, Lucio,Tardella, Paolo A.

, p. 587 - 588 (2007/10/02)

The effect of cationic surfactants in the reaction of cyclohexene and (ethoxycarbonyl)nitrene has been studied.When the counter-ion of the surfactant was bromide, the products of bromination of cyclohexene or those requiring the intermediacy of nitrene were observed.The latter were the only products if nitrate was the counter-ion of the surfactant, using N-oxy>urethan, even without added base.

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