13185-53-0 Usage
Derivative of cyclohexane
Cyclohexane-based structure
1-methylcyclohexane-1,2-dicarboxylic acid is derived from the cyclohexane structure, which is a six-carbon ring with a single methyl group attached.
Carboxylic acid functional groups
Two groups present
1-methylcyclohexane-1,2-dicarboxylic acid contains two carboxylic acid functional groups (-COOH) that contribute to its properties and reactivity.
Applications
Production of polymers and plastics, synthesis of pharmaceuticals and agricultural chemicals
1-methylcyclohexane-1,2-dicarboxylic acid is used as a building block in the production of various polymers and plastics, as well as in the synthesis of pharmaceuticals and agricultural chemicals.
Corrosion inhibitor
Prevents metal corrosion
1-methylcyclohexane-1,2-dicarboxylic acid can be used as a corrosion inhibitor, protecting metals from corrosion and extending their lifespan.
Component in coatings and adhesives
Improves performance
1-methylcyclohexane-1,2-dicarboxylic acid is used as a component in the formulation of coatings and adhesives, enhancing their performance and durability.
Physical properties
Colorless, odorless solid at room temperature
At room temperature, 1-methylcyclohexane-1,2-dicarboxylic acid is a colorless, odorless solid, which makes it suitable for various applications.
Toxicity
Relatively low
1-methylcyclohexane-1,2-dicarboxylic acid is considered to be relatively low in toxicity, which is beneficial for both human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 13185-53-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,8 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13185-53:
(7*1)+(6*3)+(5*1)+(4*8)+(3*5)+(2*5)+(1*3)=90
90 % 10 = 0
So 13185-53-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O4/c1-9(8(12)13)5-3-2-4-6(9)7(10)11/h6H,2-5H2,1H3,(H,10,11)(H,12,13)
13185-53-0Relevant academic research and scientific papers
Synthesis and alcoholysis of α-alkylated cyclopentane and cyclohexane fused succinic racemic anhydrides in the presence of chiral bases
Lerman, Lidija,Hamer?ak, Zdenko
, p. 235 - 240 (2016/01/20)
Bicyclic succinic anhydrides alkylated at the α-position have been prepared and submitted to alcoholysis in the presence of alkaloid bases. Anhydrides with a cyclopentane fused ring, open only from the less hindered side, generating monoesters of >80 % ee, whereas cyclohexane fused anhydrides undergo parallel kinetic resolution, producing both regioisomeric monoesters.
DIASTEREOSELECTIVE AND ENANTIOSELECTIVE SYNTHESIS OF 1,2-DISUBSTITUTED CYCLOALKANECARBOXALDEHYDES
Kogen, Hiroshi,Tomioka, Kiyoshi,Hashimoto, Shun-ichi,Koga, Kenji
, p. 3951 - 3956 (2007/10/02)
A highly useful method for diastereoselective and enantioselective synthesis of trans- and cis-1,2-disubstituted cycloalkanecarboxaldehydes (trans- and cis-10), useful chiral synthons having asymmetric tertiary and quaternary carbon atoms in vicinal positions in their rings, is devised starting from cycloalkenecarboxaldehydes (5). t-Leucine t-butyl ester (2.R=But), a highly effective chiral auxiliary reagent in the present method, can be recovered for recycling without any loss of optical purity.Some mechanistic explanations on the strereochemical courses of the reactions are presented.
