191354-88-8 Usage
Uses
Used in Organic Synthesis:
SUCCINIMIDYL NERVONATE is used as a synthetic building block for the creation of a wide range of organic compounds. Its application in this field is due to its ability to facilitate the formation of new chemical bonds and structures, which can be further utilized in the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
SUCCINIMIDYL NERVONATE is used as an intermediate in the synthesis of various pharmaceutical compounds. Its role in this industry is to provide a foundation for the development of new drugs with potential therapeutic applications, contributing to the advancement of medical treatments and healthcare solutions.
Used in Agrochemical Industry:
SUCCINIMIDYL NERVONATE is used as a key component in the development of agrochemicals, such as pesticides and fertilizers. Its application in this industry is aimed at enhancing crop protection and yield, thereby supporting sustainable agricultural practices and food security.
Used in Specialty Chemicals:
SUCCINIMIDYL NERVONATE is used as a vital ingredient in the production of specialty chemicals, which find applications in various sectors, including coatings, adhesives, and plastics. Its use in this industry is driven by its ability to improve the performance and properties of these materials, leading to the development of innovative products with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 191354-88-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,3,5 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 191354-88:
(8*1)+(7*9)+(6*1)+(5*3)+(4*5)+(3*4)+(2*8)+(1*8)=148
148 % 10 = 8
So 191354-88-8 is a valid CAS Registry Number.
191354-88-8Relevant academic research and scientific papers
Formation of high-axial-ratio-microstructures from natural and synthetic sphingolipids
Goldstein, Alex S.,Lukyanov, Anatoly N.,Carlson, Paul A.,Paul Yager,Gelb, Michael H.
, p. 21 - 36 (2007/10/03)
Amphiphiles that form high-axial-ratio-microstructures (HARMs) are being considered as novel materials for controlled release of drugs and other biologically functional molecules. HARMs consisting of tubules, ribbons, solid rods and helices are formed from sphingolipids by addition of water to a solution of amphiphile in DMF. Single molecular species of galactocerebroside (GalCer) containing long unsaturated fatty acid chains or natural GalCer containing mixed-length, non-hydroxy fatty acids (NFA-GalCer) or α-hydroxy fatty acids (HFA-GalCer) form cylindrical structures. In contrast, single molecular species of GalCer containing long saturated fatty acids form ribbons and helices. GalCer HARMs are typically under 100 nm in diameter and have lengths of several microns. The importance of the amide of GalCer for HARM formation was evaluated using psychosine, which forms solid fibers, whereas sphingosine and an analog of GalCer in which the amide is reduced to a secondary amine form amorphous aggregates. Single molecular species of ceramide containing long unsaturated fatty acid chains form cylindrical structures, whereas those with long saturated fatty acids form ribbons and helices. Short chain saturated ceramide also forms cylindrical structures. GalCer analogs with N-acetyl-glycine in place of the galactose form fibers whereas those with N-acetyl-proline yield amorphous material. The N-acetyl-proline-containing amphiphile can de doped into pure GalCer or NFA-GalCer without perturbing tubule formation.
