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1-Oxa-3-azaspiro[4.5]decane-2,4-dione is a cyclic compound with a unique structure, consisting of a spiro ring system that includes an oxygen atom and a nitrogen atom. This molecule features a 1-oxa (oxygen-containing) and a 3-aza (nitrogen-containing) framework, with two carbonyl groups (dione) at the 2nd and 4th positions. The compound is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its specific chemical properties and reactivity. Its synthesis and characterization are of interest to researchers, as it can be used as a building block for more complex molecules or as a chiral auxiliary in asymmetric synthesis.

7759-32-2

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7759-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7759-32-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,5 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7759-32:
(6*7)+(5*7)+(4*5)+(3*9)+(2*3)+(1*2)=132
132 % 10 = 2
So 7759-32-2 is a valid CAS Registry Number.

7759-32-2Downstream Products

7759-32-2Relevant academic research and scientific papers

A facile one-pot synthesis of 3-unsubstituted-2,4-oxazolidinediones via in situ generation of carbamates from α-hydroxyesters using trichloroacetyl isocyanate

Li, Yue H.,Zhang, Li,Tseng, Pei-San,Zhang, Yongliang,Jin, Yu,Shen, Jingkang,Jin, Jian

scheme or table, p. 790 - 792 (2009/05/07)

A convenient, high yield one-pot methodology for the synthesis of pharmaceutically interesting 3-unsubstituted-2,4-oxazolidinediones from α-hydroxyesters is described. A primary carbamate was generated in situ from the corresponding α-hydroxyester and tri

Study of the reaction between cyanohydrins and chlorosulfonyl isocyanate. A new, efficient method for the one-pot synthesis of 2,4-oxazolidinediones

Garcia,Menendez,Villacampa,Sollhuber

, p. 697 - 698 (2007/10/02)

The reaction between cyanohydrins and chlorosulfonyl isocyanate, followed by acid hydrolysis, provides and efficient route for the one-pot preparation of 5,5-disubstituted 2,4-oxazolidinediones.

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