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(1R,3S)-dimethyl cyclopentane-1,3-dicarboxylate is a cyclopentane derivative and a dicarboxylic acid ester with the molecular formula C9H14O4. It is a chemical compound that is commonly used as an intermediate in the synthesis of various drugs and organic compounds in the pharmaceutical and chemical industries. The (1R,3S) stereoisomer refers to the configuration of the molecule, which plays a significant role in determining its chemical and biological properties. Overall, (1R,3S)-dimethyl cyclopentane-1,3-dicarboxylate is a versatile compound with diverse applications in various fields.

190137-08-7

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190137-08-7 Usage

Uses

Used in Pharmaceutical Industry:
(1R,3S)-dimethyl cyclopentane-1,3-dicarboxylate is used as an intermediate for the synthesis of various drugs and organic compounds. Its unique stereochemistry and versatile chemical properties make it a valuable building block in the development of new pharmaceuticals.
Used in Chemical Industry:
(1R,3S)-dimethyl cyclopentane-1,3-dicarboxylate is used as an intermediate for the synthesis of various organic compounds. Its unique structure and reactivity make it a useful component in the production of specialty chemicals and materials.
Used in Organic Chemistry Research:
(1R,3S)-dimethyl cyclopentane-1,3-dicarboxylate is used as a research compound in organic chemistry. Its unique stereochemistry and versatile chemical properties make it an interesting subject for studying reaction mechanisms, stereoselectivity, and the development of new synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 190137-08-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,1,3 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 190137-08:
(8*1)+(7*9)+(6*0)+(5*1)+(4*3)+(3*7)+(2*0)+(1*8)=117
117 % 10 = 7
So 190137-08-7 is a valid CAS Registry Number.

190137-08-7Relevant academic research and scientific papers

Oxidative carbomethoxylation of alkenes using a Pd(II)/molybdovanadophosphate (NPMoV) system under carbon monoxide and air

Yokota, Takahiro,Sakaguchi, Satoshi,Ishii, Yasutaka

, p. 5005 - 5008 (2002)

Oxidative carbomethoxylation of cyclopentene (1) under carbon monoxide and air by the use of a catalytic amount of Pd(OAc)2 and molybdovanadophosphate (NPMoV) led to dimethyl cis-1,2-cyclopentanedicarboxylate (2) and dimethyl cis-1,3-cyclopentanedicarboxylate (3) in good yields. Total yields of 2 and 3 were found to be improved by adding a small amount of NH4Cl. Several alkenes were similarly converted into the corresponding dimethyl dicarboxylates. The role of Cl- in the present catalytic system is suggested.

Ozonolysis of Symmetrically 1,2-Disubstituted Ethylenes in HCl/Methanol Solutions: Acid Catalyzed Reactions of Primary Cleavage Products

Griesbaum, Karl,Neumeister, Joachim

, p. 2697 - 2706 (2007/10/02)

The ozonolysis of olefins in 1 M anhydrous solutions of hydrogen chloride in methanol at /= 0 deg C was investigated.Upon warm-up of the ozonolysis products, the peroxidic primary fragmentation products were converted into non peroxidic end-products by HCl-catalyzed reactions.Cyclopentene (1a) and cyclohexene (1b), e.g., afforded mixtures of the corresponding α,ω-dialdehydebis(dimethyl acetals) (8), dimethyl α,ω-dicarboxylates (9), and methyl ω-aldehyde dimethyl acetal carboxylates (10).Norbornene (1c) gave a mixture of the correspondingly substituted 1,3-cyclopentane compounds (8c - 10c), phenanthrene (22) gave a mixture of methyl 2'-formyl-2-biphenylcarboxylate (24a), 2,2'-biphenyldicarbaldehyde (24b), and dimethyl 2,2'-biphenyldicarboxylate (24c).A reaction scheme was advanced for the rationalization of the types and the distribution of the products.It was partly substantiated by model reactions.

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