13099-35-9 Usage
Uses
Used in Surfactant and Emulsifier Production:
17-BROMOHEPTADECANOIC ACID is used as a key component in the production of surfactants and emulsifiers due to its capacity to reduce the surface tension of liquids, which is crucial for the stability and performance of these products in various formulations.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 17-BROMOHEPTADECANOIC ACID serves as a building block for the synthesis of various organic compounds, contributing to the development of new drugs and therapeutic agents.
Used in Medical Research:
17-BROMOHEPTADECANOIC ACID is used as a subject of study in medical research for its potential antifungal and antibacterial properties, indicating its possible use in the development of new antimicrobial agents to combat resistant infections.
Check Digit Verification of cas no
The CAS Registry Mumber 13099-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,9 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13099-35:
(7*1)+(6*3)+(5*0)+(4*9)+(3*9)+(2*3)+(1*5)=99
99 % 10 = 9
So 13099-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H33BrO2/c18-16-14-12-10-8-6-4-2-1-3-5-7-9-11-13-15-17(19)20/h1-16H2,(H,19,20)
13099-35-9Relevant academic research and scientific papers
Synthesis and Th1-immunostimulatory activity of α-galactosylceramide analogues bearing a halogen-containing or selenium-containing acyl chain
Hossain, Md. Imran,Hanashima, Shinya,Nomura, Takuto,Lethu, Sébastien,Tsuchikawa, Hiroshi,Murata, Michio,Kusaka, Hiroki,Kita, Shunsuke,Maenaka, Katsumi
, p. 3687 - 3695 (2016/07/20)
A novel series of CD1d ligand α-galactosylceramides (α-GalCers) were synthesized by incorporation of the heavy atoms Br and Se in the acyl chain backbone of α-galactosyl-N-cerotoylphytosphingosine. The synthetic analogues are potent CD1d ligands and stimulate mouse invariant natural killer T (iNKT) cells to selectively enhance Th1 cytokine production. These synthetic analogues would be efficient X-ray crystallographic probes to disclose precise atomic positions of alkyl carbons and lipid–protein interactions in KRN7000/CD1d complexes.
