75052-75-4 Usage
Uses
Used in Flavor and Fragrance Industry:
2-Hexyl-3-MethylMaleic Anhydride is used as a synthetic building block for creating complex fragrances and flavors. Its unique chemical structure allows it to contribute to the development of novel scents and tastes, enhancing the sensory experience of various products.
Used in Insect Attractants:
2-Hexyl-3-MethylMaleic Anhydride is found as an ingredient in the volatile oils of California raisins and almond hulls. It has been identified as a possible insect attractant, making it a valuable component in the development of pest control strategies and agricultural applications.
Used in Chemical Synthesis:
Due to its reactive nature, 2-Hexyl-3-MethylMaleic Anhydride can be used as a key intermediate in the synthesis of various organic compounds. Its anhydride functionality can be utilized to form esters, amides, and other derivatives, which can be further employed in the production of pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Material Science:
2-Hexyl-3-MethylMaleic Anhydride's unique structure and properties make it a potential candidate for the development of new materials with specific characteristics. It can be used in the synthesis of polymers, coatings, and adhesives, where its reactivity and compatibility with other monomers and polymers can be exploited to create materials with tailored properties.
Check Digit Verification of cas no
The CAS Registry Mumber 75052-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,5 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75052-75:
(7*7)+(6*5)+(5*0)+(4*5)+(3*2)+(2*7)+(1*5)=124
124 % 10 = 4
So 75052-75-4 is a valid CAS Registry Number.
75052-75-4Relevant academic research and scientific papers
Regioselective monoalkylation of dimethyl alkylidenesuccinates: Simple approach to dialkyl-substituted maleic anhydrides including chaetomellic acid A
Kshirsagar, Umesh A.,Argade, Narshinha P.
, p. 1804 - 1808 (2011/07/29)
Natural and nonnatural dialkylmaleic anhydrides were readily prepared from dimethyl alkylidenesuccinates by sodium hexamethyldisilazide-induced selective monoalkylation followed by base-catalyzed hydrolysis. Georg Thieme Verlag Stuttgart - New York.
A Simple and efficient route to chaetomellic anhydride A: A potent natural ras farnesyl-protein transferase inhibitor
De Buyck, Laurent,Cagnoli, Rita,Ghelfi, Franco,Merighi, Giulia,Mucci, Adele,Pagnoni, Ugo M.,Parsons, Andrew F.
, p. 1680 - 1686 (2007/10/03)
A new and efficient approach to chaetomellic anhydride A has been devised starting from 2,2-dichloropalmitic acid. This involves the atom transfer radical cyclization of an N-alkyl-N-(3-chloro-2-propenyl)amide followed by rearrangement of the resulting trichloro-pyrrolidin-2-one.
An expeditious synthesis of chaetomellic anhydrides a and B, and analogues
Poigny, Stephane,Guyot, Michele,Samadi, Mohammad
, p. 2175 - 2177 (2007/10/03)
Chaetomellic anhydrides A and B and analogues have been prepared in one step by Barton radical decarboxylation; namely, irradiation of thiohydroxamic esters derived from carboxylic acids, in the presence of citraconic anhydride.
