130793-26-9 Usage
Description
(6R)-3-hexyl-3,4,5,6-tetrahydro-4-hydroxy-6-undecyl-2H-pyran-2-one is a pyranone, a class of organic compounds characterized by a six-membered ring with oxygen and carbon atoms. This specific compound features hexyl and undecyl side chains and a hydroxy group, which is an oxygen atom bonded to a hydrogen atom. Its unique molecular structure and properties suggest potential applications across various industries.
Uses
Used in Pharmaceutical Industry:
(6R)-3-hexyl-3,4,5,6-tetrahydro-4-hydroxy-6-undecyl-2H-pyran-2-one is used as a pharmaceutical compound for its potential therapeutic properties. The hydroxy group in its structure may allow for interactions with biopolymers and macromolecules, making it a candidate for drug development.
Used in Flavors and Fragrances Industry:
(6R)-3-hexyl-3,4,5,6-tetrahydro-4-hydroxy-6-undecyl-2H-pyran-2-one is used as a component in the flavors and fragrances industry, where its unique molecular structure could contribute to the creation of novel scents and tastes.
Used in Agrochemicals Industry:
(6R)-3-hexyl-3,4,5,6-tetrahydro-4-hydroxy-6-undecyl-2H-pyran-2-one is used as a chemical in the agrochemicals industry, possibly for the development of new pesticides or other agricultural products, taking advantage of its specific structural features.
Check Digit Verification of cas no
The CAS Registry Mumber 130793-26-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,7,9 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 130793-26:
(8*1)+(7*3)+(6*0)+(5*7)+(4*9)+(3*3)+(2*2)+(1*6)=119
119 % 10 = 9
So 130793-26-9 is a valid CAS Registry Number.
130793-26-9Relevant articles and documents
Tetrahydrolipstatin: Thermal and hydrolytic degradation
Stalder,Schneider,Oesterhelt
, p. 1022 - 1036 (2007/10/02)
The thermal and hydrolytic degradation of tetrahydrolipstatin (THL, 1) was investigated. All main degradation products were isolated, characterized, and synthesized. Labile intermediates unavailable to isolation were detected and identified by GC/MS analysis of their silylated derivatives, and whenever possible, compared with independently prepared reference compounds. The identified degradation products represent at least 97% of the total degradation mixture. Two main reaction pathways are proposed. Pharmacological data are reported for the degradation mixture and the main degradation products.
