50483-99-3 Usage
Description
1,2-Cyclopentanedicarboxylic acid is an organic compound with the molecular formula C7H10O4. It features a cyclopentane ring with two carboxylic acid groups attached to the 1 and 2 positions, respectively. This dicarboxylic acid is known for its potential applications in various industries due to its unique chemical structure and properties.
Uses
Used in Chemical Synthesis:
1,2-Cyclopentanedicarboxylic acid is used as an intermediate in the synthesis of trans-1,2-Dimethylcyclopentane (D464925) for [application reason] its role in the production of this specific hydrocarbon.
Used in Geological Studies:
In the field of geology, 1,2-Cyclopentanedicarboxylic acid is used as a chemical marker for [application reason] determining the maturation history of sedimentary rocks, as trans-1,2-Dimethylcyclopentane, which it helps synthesize, is one of the hydrocarbons found in these rocks.
Please note that the provided materials only mention the use of 1,2-Cyclopentanedicarboxylic acid as an intermediate in the synthesis of trans-1,2-Dimethylcyclopentane. If there are other applications or uses in different industries, they are not covered in the provided materials.
Check Digit Verification of cas no
The CAS Registry Mumber 50483-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,8 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50483-99:
(7*5)+(6*0)+(5*4)+(4*8)+(3*3)+(2*9)+(1*9)=123
123 % 10 = 3
So 50483-99-3 is a valid CAS Registry Number.
50483-99-3Relevant articles and documents
Method for synthesizing cyclopentyl imide
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Paragraph 0016; 0017; 0018; 0019; 0020, (2017/07/19)
The invention relates to a method for synthesizing cyclopentyl imide. The method comprises the following steps: reacting a raw material 1,2-cyclopentanediamide with an alkali liquid to generate 1,2-cyclopentanediacid, and reacting the 1,2-cyclopentanediacid with methanamide to generate the cyclopentyl imide. The synthesis method greatly reduces the cyclopentyl imide synthesis temperature to make the reaction mildly proceed, so the high temperature problem in the prior art is solved, the safety in the production process is improved, and energy saving and consumption reduction are realized; and the method has the advantages of liquid and homogenous synthesis system, stable reaction and quality, low temperature reaction conditions, no generation of coking, oxidation or carbonizing waste resides or other impurities, improvement of the quality of the above product, realization of the continuous primary yield reaching 90% or above and being about 10-30% higher than that of present technologies, stable reaction technology conditions, easiness in control, and high reaction conversion rate.
Preparation of Small Ring Carbocycles via Intramolecular Oxidative Coupling of Bisenolates Derived from α,ω-Diesters
Babler, James H.,Sarussi, Steven J.
, p. 3462 - 3464 (2007/10/02)
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Biosynthesis of brefeldin A
Handschin,Sigg,Tamm
, p. 1943 - 1965 (2007/10/05)
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