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Methyl 1,4-dioxaspiro[4.4]nonane-7-carboxylate is an organic chemical compound characterized by its molecular formula C10H16O4. It is a spiro compound, featuring a bicyclic ring system with a shared carbon atom between the two rings. methyl 1,4-dioxaspiro[4.4]nonane-7-carboxylate is widely recognized for its role as a building block in the synthesis of various organic molecules and pharmaceuticals, contributing to the development of new drugs and materials. As a colorless liquid with a slightly fruity odor, it requires careful storage and handling under inert gas atmospheres to prevent oxidation and degradation.

77250-34-1

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77250-34-1 Usage

Uses

Used in Organic Chemistry:
Methyl 1,4-dioxaspiro[4.4]nonane-7-carboxylate is utilized as a key intermediate in the synthesis of complex organic molecules, facilitating the creation of a diverse range of chemical compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, methyl 1,4-dioxaspiro[4.4]nonane-7-carboxylate serves as a crucial component in the development of new drugs, leveraging its structural properties to enhance the efficacy and functionality of medicinal compounds.
Used in Material Science:
Methyl 1,4-dioxaspiro[4.4]nonane-7-carboxylate is employed in the field of material science to develop innovative materials with unique properties, such as improved stability and reactivity, by incorporating its molecular structure into the design of these materials.

Check Digit Verification of cas no

The CAS Registry Mumber 77250-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,5 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 77250-34:
(7*7)+(6*7)+(5*2)+(4*5)+(3*0)+(2*3)+(1*4)=131
131 % 10 = 1
So 77250-34-1 is a valid CAS Registry Number.

77250-34-1Downstream Products

77250-34-1Relevant academic research and scientific papers

Facile synthesis of 2-azaspiro[3.4]octane

Ramesh, Subbiah,Balakumar, Ramadas,Rizzo, John R.,Zhang, Tony Y.

, p. 3056 - 3065 (2019/03/21)

Our annulation strategy utilized for the synthesis of 2-azaspiro[3.4]octane is explained. Three successful routes for the synthesis were developed. One of the approaches involved annulation of the cyclopentane ring and the remaining two approaches involved annulation of the four membered ring. All three approaches employ readily available starting materials with conventional chemical transformations and minimal chromatographic purifications to afford the title compound. The merits and limitations of the three approaches are also discussed.

Hydroxypurine compound and use thereof

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Paragraph 0232; 0233; 0234; 0235, (2016/10/08)

The invention discloses a hydroxypurine compound and a use of the hydroxypurine compound as a PDE2 or TNFa inhibitor and concretely discloses a compound shown in the formula (I) and its tautomer or pharmaceutically acceptable salt.

A FACILE STEREOSELECTIVE SYNTHESIS OF +/- SESBANINE

Wanner, Martinus J.,Koomen, Gerrit-Jan,Pandit, Upendra K.

, p. 377 - 379 (2007/10/02)

10-Dehydrosesbanine (4), prepared via a sequence in which the tricyclic spiro cyclopentano-2,7-naphthyridine ring system is prepared by condensation of 3-(ethylenedioxy)cyclopentanecarboxylate ester anion with N-benzylnicotinamide, is stereoselectively re

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