117168-59-9 Usage
Description
(2S,3S,4R)-2-Azido-1,3,4-octadecanetriol is a chiral azido alcohol with a unique molecular structure characterized by three stereocenters and an azide functional group. It is a white solid with specific chemical properties that make it suitable for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
(2S,3S,4R)-2-Azido-1,3,4-octadecanetriol is used as a chiral building block for the synthesis of complex organic molecules and pharmaceutical compounds. Its unique stereochemistry and azide functionality allow for the development of innovative drugs with improved efficacy and selectivity.
Used in Immunology Research:
(2S,3S,4R)-2-Azido-1,3,4-octadecanetriol is used as a photo-crosslinking agent to control immune activity with light. This property enables researchers to study the immunostimulatory activity of α-galactosylceramide and other immune modulators, providing valuable insights into the regulation of immune responses.
Used in Materials Science:
(2S,3S,4R)-2-Azido-1,3,4-octadecanetriol is used as a precursor for the synthesis of functional polymers and materials with tailored properties. Its azide group can be utilized in click chemistry reactions, allowing for the efficient and selective formation of complex polymeric structures with potential applications in various fields, such as drug delivery, tissue engineering, and nanotechnology.
Check Digit Verification of cas no
The CAS Registry Mumber 117168-59-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,1,6 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 117168-59:
(8*1)+(7*1)+(6*7)+(5*1)+(4*6)+(3*8)+(2*5)+(1*9)=129
129 % 10 = 9
So 117168-59-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H37N3O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-17(23)18(24)16(15-22)20-21-19/h16-18,22-24H,2-15H2,1H3/t16-,17+,18-/m0/s1
117168-59-9Relevant articles and documents
Synthesis of ganglioside Hp-s1
Chen, Wan-Shin,Sawant, Ratnnadeep C.,Yang, Shih-An,Liao, Ying-Ju,Liao, Jung-Wei,Badsara, Satpal Singh,Luo, Shun-Yuan
, p. 47752 - 47761 (2014)
A simple protocol for the synthesis of a ganglioside Hp-s1 (1) starting from commercially available phytosphingosine, sialic acid, and d-glucose is described. This synthesis involved a glycosylation reaction of a phytosphingosine derived acceptor with a h
GLYCOLIPID CONTROLLABLE OF IMMUNE ACTIVITY WITH LIGHT
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Paragraph 0078, (2020/08/11)
PROBLEM TO BE SOLVED: To provide means of improving immunostimulation activity of α-galactosylceramide. SOLUTION: The invention provides a compound represented by the general formula (I) in the figure, where Ar represents an aryl group that may be substituted with substituents such as a phenyl group, or a heteroaryl group that may be substituted with substituents, and n represents an integer from 4 to 12. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT
A versatile synthesis of αGalCer and its analogues exploiting a cyclic carbonate as phytosphingosine 3,4-diol protecting group
Panza, Luigi,Compostella, Federica,Imperio, Daniela
, p. 50 - 57 (2018/11/26)
A convenient synthetic strategy to αGalCer and some relevant analogues by using a handily protected phytosphingosine is reported here. The conversion of the phytosphingosine amino group to azide and the protection of 3,4-diol as cyclic carbonate group, cl