139003-96-6 Usage
General Description
1,2-Propanediol,3-(2-ethoxyphenoxy)-,(R)-(9CI) is a chemical compound that is classified as a diol, meaning it contains two hydroxyl groups. It is also known by the name propylene glycol phenyl ether. 1,2-Propanediol,3-(2-ethoxyphenoxy)-,(R)-(9CI) is commonly used as a solvent in various industrial and consumer products, including paints, coatings, and adhesives. It is known for its ability to dissolve a wide range of substances, making it valuable in many different industrial applications. Additionally, it is often used as a chemical intermediate in the production of other compounds. Overall, 1,2-Propanediol,3-(2-ethoxyphenoxy)-,(R)-(9CI) is an important and versatile chemical compound with a wide range of uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 139003-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,0,0 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 139003-96:
(8*1)+(7*3)+(6*9)+(5*0)+(4*0)+(3*3)+(2*9)+(1*6)=116
116 % 10 = 6
So 139003-96-6 is a valid CAS Registry Number.
139003-96-6Relevant articles and documents
Spontaneous resolution among chiral glycerol derivatives: crystallization features of ortho-alkoxysubstituted phenyl glycerol ethers
Bredikhin, Alexander A.,Bredikhina, Zemfira A.,Zakharychev, Dmitry V.,Konoshenko, Larisa V.
, p. 1964 - 1970 (2008/02/13)
Five chiral arylglycerol ethers 2-R-C6H4-O-CH2CH(OH)CH2OH (R = OMe, OEt, OPrn, OPri, OBut) have been prepared in racemic and enantiopure form. The melting points and enthalpies of fusion of every species were measured by differential scanning calorimetry. Binary phase diagrams were reconstructed for the whole family, the entropies of the mixing of the enantiomers in the liquid state, and Gibbs free energy of formation of the racemic compound, as well as Pettersson i-values were derived from the thermal data. The differences in the phase behavior of the investigated compounds were associated with the conformations of the alkoxy fragments.
