134254-33-4 Usage
Physical form
Clear, colorless liquid with a mild odor
Solubility
Soluble in water and most organic solvents
Uses
Commonly used as a solvent and surfactant in various industrial and household products, including cleaning products, coatings, and paints, as well as in agriculture, textiles, and personal care products
Other functions
Used as a coupling agent to enhance the solubility of various substances in water-based solutions
Toxicity
Low acute toxicity and generally considered safe for use in consumer products when used as directed
Check Digit Verification of cas no
The CAS Registry Mumber 134254-33-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,2,5 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 134254-33:
(8*1)+(7*3)+(6*4)+(5*2)+(4*5)+(3*4)+(2*3)+(1*3)=104
104 % 10 = 4
So 134254-33-4 is a valid CAS Registry Number.
134254-33-4Relevant academic research and scientific papers
Synthesis and some features of phase behavior of chiral p-alkoxyphenyl glycerol ethers
Fayzullin,Antonovich,Zakharychev,Bredikhina,Kurenkov,Bredikhin
, p. 202 - 209 (2015/04/14)
A series of (S)-3-(4-alkoxyphenoxy)propane-1,2-diols was prepared with the enantiomeric excess 86-92% by Sharpless asymmetric dihydroxylation of 1-alkoxy-4-allyloxybenzenes with an AD-mix-β mixture. R-Enantiomers with enantiomeric excess 97-99% and racemic samples were obtained by reaction of sodium p-substituted phenolates with (R)- and rac-3-chloropropane-1,2-diol. The phase behavior of racemates and scalemates in the produced homolog series of glycerol aryl ethers with hydrocarbon substituents of various length was examined by means of thermomicroscopy. The higher memberes of the homolog series of both racemic and scalemic diols undergo at heating an enantiotropic phase transition to a smectic liquid crystal phase.
