7226-88-2 Usage
Uses
Used in Plastics and Rubber Industry:
2,6-dicyclohexyl-p-cresol is used as an antioxidant for [application reason] to prevent the degradation of plastics and rubber products, thereby extending their shelf life and maintaining their physical and chemical properties.
Used in Personal Care Products:
2,6-dicyclohexyl-p-cresol is used as a preservative in personal care products such as lotions and creams for [application reason] to prevent the oxidation of fatty acids and other sensitive ingredients, ensuring the stability and effectiveness of these products.
It is important to handle 2,6-dicyclohexyl-p-cresol with care, as it may pose health hazards if not handled properly.
Check Digit Verification of cas no
The CAS Registry Mumber 7226-88-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,2 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7226-88:
(6*7)+(5*2)+(4*2)+(3*6)+(2*8)+(1*8)=102
102 % 10 = 2
So 7226-88-2 is a valid CAS Registry Number.
InChI:InChI=1/C22H28N4O3S/c1-14-23-30-22(21(5,6)7)16(20(2,3)4)13-24-18(27)25(15-11-9-8-10-12-15)19(28)26(24)17(22)29-14/h8-13,17H,1-7H3/q+2
7226-88-2Relevant articles and documents
A new convenient Friedel-Crafts alkylation of aromatic compounds with secondary alcohol methanesulfonates in the presence of scandium(III) trifluoromethanesulfonate or trifluoromethanesulfonic acid as the catalyst
Kotsuki, Hiyoshizo,Ohishi, Takeshi,Inoue, Motoshi,Kojima, Tomoyuki
, p. 603 - 606 (2007/10/03)
Scandium(III) triflate and triflic acid were both found to be efficient catalysts for the Friedel-Crafts alkylation of aromatic compounds using methanesulfonates derived from secondary alcohols as alkylating agents.
ORTHO-ALKYLATION OF o-, m-, AND p-CRESOLS WITH CYCLOHEXENE IN THE PRESENCE OF ALUMINUM CRESOLATES
Kozlikovskii, Ya. B.,Koshchii, V. A.,Butov, S. A.,Sokolova, A. V.
, p. 1702 - 1707 (2007/10/02)
The reaction of o-, m-, and p-cresols with cyclohexene in the presence of the corresponding aluminum cresolates leads to mixtures of ethers and phenols, in which the ortho-alkylation products, formed with yields of 75-85percent, predominate.