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4209-22-7

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4209-22-7 Usage

General Description

1-Bromotriacontane is a long-chain alkane with the molecular formula C33H68Br. It is a colorless solid at room temperature and is insoluble in water, but soluble in organic solvents. 1-bromotriacontane is primarily used in the production of surfactants, lubricants, and coatings. It also has potential applications in the field of medicine and as a chemical intermediate in organic synthesis. This chemical is also known for its ability to form self-assembled monolayers on different substrates and has potential applications in the field of nanotechnology. It is important to handle 1-bromotriacontane with caution as it is considered to be a hazardous chemical, with potential health hazards including skin and respiratory irritation, and should be used with appropriate safety measures.

Check Digit Verification of cas no

The CAS Registry Mumber 4209-22-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,0 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4209-22:
(6*4)+(5*2)+(4*0)+(3*9)+(2*2)+(1*2)=67
67 % 10 = 7
So 4209-22-7 is a valid CAS Registry Number.
InChI:InChI=1/C30H61Br/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31/h2-30H2,1H3

4209-22-7Upstream product

4209-22-7Relevant articles and documents

Correlation of anti-HIV potency with lipophilicity in a series of cosalane analogs having normal alkenyl and phosphodiester chains as cholestane replacements

Keyes, Robert F.,Golebiewski, W. Marek,Cushman, Mark

, p. 508 - 514 (2007/10/03)

In order to define the role of the cholestane moiety in the anti-HIV agent cosalane, a series of cosalane analogs was synthesized in which the cholestane ring system was replaced by normal alkenyl and phosphodiester substituents having varied chain lengths and lipophilicities. The compounds containing simple alkenyl substituents were found to be more potent as inhibitors of the cytopathic effect of HIV-1 in cell culture than the phosphodiesters. In addition, the potencies of the alkene congeners correlated positively with chain length and lipophilicity of the alkene. The results indicate that the cholestane moiety of cosalane functions as a lipophilic accessory appendage to escort the dichlorodisalicylmethane pharmacophore to a lipid environment.

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