1883-88-1 Usage
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
Cyclopentanecarboxylic acid, 2-hydroxy-, transis utilized as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique trans isomer configuration and functional groups make it a valuable building block for the development of new drugs and pesticides.
Used in Organic Chemistry as a Chiral Building Block:
The trans isomer configuration of Cyclopentanecarboxylic acid, 2-hydroxy-, transmakes it particularly useful as a chiral building block in organic chemistry. It can be employed in asymmetric synthesis and the preparation of enantiomerically pure compounds, which are essential in the pharmaceutical industry for the development of more effective and safer drugs.
Used in Flavor and Fragrance Production:
Cyclopentanecarboxylic acid, 2-hydroxy-, transhas potential applications in the production of flavors and fragrances. Its unique chemical structure and properties can contribute to the creation of novel and complex scents, enhancing the sensory experience in various consumer products such as perfumes, cosmetics, and food products.
Check Digit Verification of cas no
The CAS Registry Mumber 1883-88-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,8 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1883-88:
(6*1)+(5*8)+(4*8)+(3*3)+(2*8)+(1*8)=111
111 % 10 = 1
So 1883-88-1 is a valid CAS Registry Number.
1883-88-1Relevant academic research and scientific papers
SYNTHESIS AND PROPERTIES OF 2-DIAZO-1,3-DICARBONYL COMPOUNDS. V. SYNTHESIS AND 1,2-NUCLEOPHILIC REARRANGEMENTS OF SOME 2-DIAZO-3-HYDROXY-1-CYCLOHEXANONES
Nikolaev, V. A.,Zhdanova, O. V.,Korobitsyna, I. K.
, p. 488 - 498 (2007/10/02)
2-Diazo-3-hydroxy, 2-diazo-3-hydroxy-5,5-dimethyl, and 2-diazo-3-hydroxy-4,4,6,6-tetramethyl-1-cyclohexanones were obtained by reduction of 2-diazo 1,3-diketones of the cyclohexane series, and their spectral characteristics were determined.Photolytic, catalytic, and thermal elimination of nitrogen in these diazo compounds is only accompanied by 1,2-nucleophilic rearrangements.During photolysis of the diazohydroxycyclohexanones in an aqueous medium the main reaction path is a Wolff rearrangement, i.e., ring contraction with the formation of hydroxy and unsaturated acids of the cyclopentane series and some of their derivatives.Acid decomposition of the diazohydroxycyclohexanones leads mainly to an alkyl shift as a result of which (hydroxymethylene)cyclopentanones are formed with ring contraction.
