53670-54-5 Usage
Uses
Used in Food and Fragrance Industry:
3-Mercapto-2,5-hexanedione is used as a chemical intermediate for the production of food and fragrance additives. Its strong nucleophilic properties allow for the addition of sulfur to double bonds, contributing to the development of unique scents and flavors.
Used in Pharmaceutical Industry:
3-Mercapto-2,5-hexanedione is used as a building block in the synthesis of pharmaceuticals. Its reactivity and ability to form stable compounds make it a valuable component in the creation of new drugs and medicinal compounds.
Used in Organic Chemistry:
3-Mercapto-2,5-hexanedione is used as a reagent in various organic chemistry reactions. Its strong nucleophilic properties enable the addition of sulfur to double bonds, facilitating the formation of new chemical bonds and the synthesis of complex organic compounds.
Used as a Chelating Agent:
3-Mercapto-2,5-hexanedione is used as a chelating agent, capable of binding to metal ions and forming stable complexes. This property makes it useful in analytical chemistry and biochemistry for the separation and analysis of metal ions.
Used in Analytical Chemistry:
3-Mercapto-2,5-hexanedione is used in analytical chemistry for its potential applications in the separation and analysis of metal ions. Its chelating properties allow for the selective binding and detection of specific metal ions, enhancing the accuracy and efficiency of analytical processes.
Used in Biochemistry:
3-Mercapto-2,5-hexanedione has potential applications in biochemistry due to its ability to interact with metal ions and other biomolecules. Its chelating properties can be utilized in the study of metalloenzymes and the development of new biocatalysts and biosensors.
Check Digit Verification of cas no
The CAS Registry Mumber 53670-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,7 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53670-54:
(7*5)+(6*3)+(5*6)+(4*7)+(3*0)+(2*5)+(1*4)=125
125 % 10 = 5
So 53670-54-5 is a valid CAS Registry Number.
53670-54-5Relevant articles and documents
Process for producing 2-thia substituted 1,4 diones
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, (2008/06/13)
Process for producing 3-thia substituted alkane 1,4 diones comprising the steps of: I. Providing a 2-ene-1,4 dione having the structure: SPC1 Ii. Intimately admixing said 2-ene-1,4 dione with a sulfur compound having the formula: thereby providing a substituted or sunsubstituted 2-thia substituted alkane 1,4 dione having the structure: SPC2 Wherein R3 is selected from the group consisting of acyl and royl, wherein R2 is lower alkyl; and wherein R1, R4 and r6 are the same or different and are selected from the group consisting of hydrogen and lower alkyl; wherein when R1 is hydrogen, the reaction (ii) is carried out in the presence of an organic base; and wherein when R1 is lower alkyl, the reaction (ii) is carried out in the absence of catalyst. Examples of such organic bases are piperidine, pyridine, triethyl amine, quinoline or alpha-picoline.
Process for producing 2-mercapto-1,4-diones
-
, (2008/06/13)
Process for producing 2-mercapto alkane-1,4-diones comprising the steps of: I. Providing a 2-ene-1,4-dione having the structure: STR1 ii. Intimately admixing said 2-ene-1,4-dione with a sulfur compound having the formula: thereby providing a substituted or unsubstituted 2-thia substituted alkane 1,4 dione having the structure: STR2 iii. Hydrolyzing said 2-thia substituted 1,4 dione thereby forming a 2-mercapto alkane-1,4-dione having the structure: STR3 wherein R3 is selected from the group consisting of acyl and aroyl, wherein R2 is lower alkyl; and wherein R4 and R6 are the same or different and are selected from the group consisting of hydrogen and lower alkyl; wherein when R1 is hydrogen, the reaction (ii) is carried out in the presence of an organic base; and wherein when R1 is lower alkyl, the reaction (ii) is carried out in the absence of catalyst or in the presence of catalyst. Examples of such organic bases are piperidine, pyridine, triethyl amine, quinoline or alpha-picoline.
