1599-67-3 Usage
Description
1-DOCOSANOL, also known as behenyl alcohol, is an alkene that is docosane with an unsaturation at position 1. It is a metabolite observed in cancer metabolism and is a long-chain alkene found in the aerial parts of the plant Origanum vulgare. It is used as an active ingredient in the treatment of herpes simplex labialis and serves as a useful building block in various applications.
Uses
Used in Pharmaceutical Industry:
1-DOCOSANOL is used as an antiviral agent for the treatment of herpes simplex labialis, providing relief from the symptoms and shortening the duration of the outbreak.
Used in Cosmetic Industry:
1-DOCOSANOL, under the brand name Abreva (GlaxoSmithKline), is used as an ingredient in the cosmetic industry, specifically for its antiviral properties in the treatment of herpes labialis.
Used in Chemical Industry:
As a long-chain alkene and a lipophilic component, 1-DOCOSANOL is used as a building block in the chemical industry for the synthesis of various compounds and materials.
Used in Cancer Metabolism Research:
1-DOCOSANOL, being a metabolite observed in cancer metabolism, is used in research to better understand the metabolic processes in cancer cells and potentially develop new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 1599-67-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1599-67:
(6*1)+(5*5)+(4*9)+(3*9)+(2*6)+(1*7)=113
113 % 10 = 3
So 1599-67-3 is a valid CAS Registry Number.
InChI:InChI=1/C22H46O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23/h23H,2-22H2,1H3
1599-67-3Relevant articles and documents
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Sharpless,K.B.,Flood,T.C.
, p. 370 - 371 (1972)
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Phase-Transfer Synthesis of Monoalkyl Ethers of Oligoethylene Glycols
Gibson, Thomas
, p. 1095 - 1098 (2007/10/02)
The effects of catalyst, temperature, solvent, and reagent ratios on the phase-transfer-catalyzed Williamson ether synthesis of monoalkyl ethers of oligoethylene glycols have been studied.A convenient method has been developed which gives reproducibly high yields of pure monoethers in the presence of aqueous sodium hydroxide.
