102013-72-9 Usage
Description
3,6,9,12,15,18,21,24,27-Nonaoxaoctacosanoic acid is a long-chain carboxylic acid with multiple hydroxyl groups, which can form stable amide bonds with primary amine groups in the presence of activators. Its hydrophilic nature increases solubility in aqueous media, making it a versatile compound for various applications.
Uses
Used in Pharmaceutical Industry:
3,6,9,12,15,18,21,24,27-Nonaoxaoctacosanoic acid is used as a building block for the synthesis of complex molecules, such as drugs and drug delivery systems, due to its ability to form stable amide bonds with primary amine groups.
Used in Cosmetics Industry:
3,6,9,12,15,18,21,24,27-Nonaoxaoctacosanoic acid is used as an emulsifying agent and solubilizer in the formulation of cosmetics, taking advantage of its hydrophilic nature and ability to form stable bonds with other molecules.
Used in Research and Development:
3,6,9,12,15,18,21,24,27-Nonaoxaoctacosanoic acid is used as a research tool for studying the properties and interactions of long-chain carboxylic acids, as well as their potential applications in various fields, including drug development and material science.
Used in Material Science:
3,6,9,12,15,18,21,24,27-Nonaoxaoctacosanoic acid can be used as a component in the development of novel materials, such as hydrogels or polymers, due to its ability to form stable bonds and its hydrophilic nature.
Check Digit Verification of cas no
The CAS Registry Mumber 102013-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,0,1 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102013-72:
(8*1)+(7*0)+(6*2)+(5*0)+(4*1)+(3*3)+(2*7)+(1*2)=49
49 % 10 = 9
So 102013-72-9 is a valid CAS Registry Number.
102013-72-9Relevant articles and documents
o-Nitrobenzyl photoremovable groups with fluorescence uncaging reporting properties
Abou Nakad,Bolze,Specht
, p. 6115 - 6122 (2018)
o-Nitrobenzyl (o-NB) derivatives are the most widely applied photoremovable groups for the study of dynamic biological processes. By introducing different substituents to the benzylic position we were able to generate a fluorescence signal upon irradiatio
CONJUGATES OF A CELL-BINDING MOLECULE WITH CAMPTOTHECIN ANALOGS
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Page/Page column 157, (2021/10/30)
Provided are conjugates of camptothecin analogs with a cell-binding molecule of formula (I), wherein R1, R2, R3, R4, R5, X, L, n, m, T and ----- are defined herein. It also provides methods of making the conjugates of camptothecin analogs to a cell-binding agent, as well as methods of using the conjugates in targeted treatment of cancer, infection, and immunological disorders.
A CONJUGATE OF AN AMANITA TOXIN WITH BRANCHED LINKERS
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Page/Page column 139, (2020/08/22)
Provided herein is the conjugation of an amanita toxin compound to a cell-binding molecule with branched linkers for having better targeted treatment of abnormal cells. It also relates to a branched-linkage method of conjugation of an amanita molecule to a cell-binding ligand, as well as methods of using the conjugate in targets treatment of cancer, infection and autoimmune disease.
