59219-70-4 Usage
Uses
Used in Pharmaceutical Industry:
DODECYLTETRADECANOL is used as a synthetic building block for the creation of muramyldipeptide lipophilic derivatives. These derivatives are essential in the development of new drugs and therapies, particularly in the field of immunology, as they can potentially modulate immune responses and target specific diseases.
Used in Chemical Synthesis:
In the chemical synthesis industry, DODECYLTETRADECANOL is utilized as a key component in the production of various compounds, such as surfactants, emulsifiers, and other specialty chemicals. Its lipophilic nature makes it a valuable addition to the synthesis process, enhancing the properties of the final products.
Used in Cosmetics Industry:
DODECYLTETRADECANOL is also employed in the cosmetics industry as an ingredient in the formulation of skincare and hair care products. Its ability to improve the texture and feel of these products, as well as its potential moisturizing and emollient properties, make it a popular choice for cosmetic manufacturers.
Check Digit Verification of cas no
The CAS Registry Mumber 59219-70-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,2,1 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59219-70:
(7*5)+(6*9)+(5*2)+(4*1)+(3*9)+(2*7)+(1*0)=144
144 % 10 = 4
So 59219-70-4 is a valid CAS Registry Number.
59219-70-4Relevant academic research and scientific papers
Impact of substitution pattern and chain length on the thermotropic properties of alkoxy-substituted triphenyl-tristriazolotriazines
Detert, Heiner,Glang, Stefan,Haspel, Tobias,Lehmann, Matthias,Limbach, Daniel,Rieth, Thorsten,Schupp, Niklas,Sperner, Marcel,Tober, Natalie,Wicker, Philipp
supporting information, (2021/06/14)
Tristriazolotriazines (TTTs) with a threefold alkoxyphenyl substitution were prepared and studied by DSC, polarized optical microscopy (POM) and X-ray scattering. Six pentyloxy chains are sufficient to induce liquid-crystalline behavior in these star-shap
The synthesis of glycosides of 2-acetamido-2-deoxyglucose catalyzed by mercuric iodide
Zemlyakov,Kur'yanov,Sidorova,Chirva
, p. 551 - 558 (2007/10/03)
The glycosylation of various alcohols with peracetylated α-D-glucosaminyl chloride catalyzed with mercuric iodide was studied along with the dependence of the reaction course on temperature, solvent, and quantity of catalyst. At room temperature, only β-glycosides of peracetylated N-acetylglucosamine were shown to result in dichloroethane or nitromethane with high yields. At 90-95°C, anomerization was observed, which led to the corresponding α-glycosides. The possibility of the synthesis of disaccharides with the β1→6 bond catalyzed by mercuric iodide was demonstrated.
