133604-58-7 Usage
Description
2,5,8,11,14,17,20,23,26,29,32,35,38,41,44,47-Hexadecaoxanonatetracontan-49-ol is a complex organic compound with a long hydrocarbon chain and multiple hydroxyl groups. It is characterized by its unique structure, which consists of 49 carbon atoms and 16 oxygen atoms, arranged in a specific pattern of hydroxylation. 2,5,8,11,14,17,20,23,26,29,32,35,38,41,44,47-Hexadecaoxanonatetracontan-49-ol has potential applications in various fields due to its structural properties and reactivity.
Uses
Used in Chemical Synthesis:
2,5,8,11,14,17,20,23,26,29,32,35,38,41,44,47-Hexadecaoxanonatetracontan-49-ol is used as a building block for the synthesis of various complex organic molecules, such as surfactants, detergents, and other specialty chemicals. Its multiple hydroxyl groups allow for further functionalization and modification, making it a versatile starting material for the development of new compounds with specific properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,5,8,11,14,17,20,23,26,29,32,35,38,41,44,47-Hexadecaoxanonatetracontan-49-ol can be used as a key intermediate in the synthesis of bioactive molecules, such as drugs targeting specific receptors or enzymes. Its unique structure and reactivity can be exploited to design and develop novel therapeutic agents with improved efficacy and selectivity.
Used in Cosmetics Industry:
2,5,8,11,14,17,20,23,26,29,32,35,38,41,44,47-Hexadecaoxanonatetracontan-49-ol can be used as an ingredient in the formulation of cosmetics and personal care products. Its hydrophilic nature and ability to form micelles or other self-assembled structures can enhance the solubility and delivery of active ingredients, improving the performance and efficacy of these products.
Used in Material Science:
In the field of material science, 2,5,8,11,14,17,20,23,26,29,32,35,38,41,44,47-Hexadecaoxanonatetracontan-49-ol can be used to develop novel materials with specific properties, such as self-assembly, amphiphilic behavior, or controlled release of active agents. Its unique structure and reactivity can be utilized to create materials with tailored properties for various applications, including drug delivery, sensors, and environmental remediation.
Check Digit Verification of cas no
The CAS Registry Mumber 133604-58-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,6,0 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 133604-58:
(8*1)+(7*3)+(6*3)+(5*6)+(4*0)+(3*4)+(2*5)+(1*8)=107
107 % 10 = 7
So 133604-58-7 is a valid CAS Registry Number.
133604-58-7Relevant articles and documents
Monodisperse oligoethylene glycols modified Camptothecin, 10-Hydroxycamptothecin and SN38 prodrugs
Deng, Tao,Mao, Xianglan,Xiao, Yan,Yang, Zhigang,Zheng, Xing,Jiang, Zhong-Xing
, p. 581 - 584 (2019/01/04)
Camptothecin, which represents a class of natural products with high anticancer activity, suffers low water solubility which hampers its clinic application. To address this issue, monodisperse polyethylene glycols were employed to modify this class of natural products, including Camptothecin, 10-Hydroxycamptothecin, and SN38. Through selective modification with a series of monodisperse polyethylene glycols, 31 Camptothecin derivatives, including 9 ethers and 22 carbonates, were prepared using a macrocyclic sulfate-based strategy with high efficacy. Monodisperse polyethylene glycols modification provided the Camptothecin derivatives with high purity and fine-tunable water solubility. Through the physicochemical and biological assays, a few novel prodrugs with good solubility, cytotoxicity, and valuable drug release profile were identified as promising anticancer drug candidates.
High-purity discrete PEG-oligomer crystals allow structural insight
French, Alister C.,Thompson, Amber L.,Davis, Benjamin G.
supporting information; experimental part, p. 1248 - 1252 (2009/06/30)
To great (monodisperse) lengths: An improved synthesis of purer ethylene glycol (EG) oligomers allows access to 16- and 32-mers pure enough for multiple incorporation, and also to the longest (48-mer) discrete EG oligomer yet reported. The high purity enables the first crystallizations and hence the first glimpses of secondary 310-helical PEG structures.
