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2-t-Butyl-4-t-butoxyphenol is a chemical compound with the molecular formula C16H26O. It is a derivative of phenol, featuring two t-butyl groups attached to the 2nd and 4th carbon atoms of the phenol ring, with a t-butoxy group attached to the 4th carbon atom. 2-t-Butyl-4-t-butoxyphenol is primarily used as an antioxidant in various industrial applications, including rubber, plastics, and lubricants, to prevent oxidation and degradation. It is also known for its ability to extend the shelf life of these materials by inhibiting the formation of peroxides and other harmful byproducts. Due to its effectiveness and stability, 2-t-Butyl-4-t-butoxyphenol is a valuable component in the manufacturing of various products that require protection against oxidative stress.

2467-52-9

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2467-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2467-52-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,6 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2467-52:
(6*2)+(5*4)+(4*6)+(3*7)+(2*5)+(1*2)=89
89 % 10 = 9
So 2467-52-9 is a valid CAS Registry Number.

2467-52-9Downstream Products

2467-52-9Relevant academic research and scientific papers

Elaboration on the Electronics of Salen Manganese Nitrides: Investigations into Alkoxy-Substituted Ligand Scaffolds

Hein, Nicholas M.,Macneil, Gregory A.,Storr, Tim

supporting information, p. 16895 - 16905 (2021/11/18)

The ligand electronics of salen manganese nitride complexes directly influence the locus of oxidation and, thus, the reactivity of the resulting oxidized species. This work investigates the influence of tert-butoxy, isopropoxy, and methoxy substituents on

p-di-t-butoxybenzene

Carman, Raymond M.,Kanizaj, Nicholas,Taylor, Richard J.K.

, p. 515 - 516 (2007/10/03)

p-Di-t-butoxybenzene (1) [p-di-tert-butoxybenzene; benzene, 1,4-di-tert-butoxy-; 1,4-bis(1,1-dimethylethoxy)benzene; 1,4-benzenediol (or benzene-1,4-diol) di-tert-butyl ether; Chem. Abstr. number 15360-01-7] does not have the physical properties ascribed to it in the Dictionary of Organic Compounds, where it has been mistaken for 2,5-di-t-butylhydroquinone (4).

Enantioselective epoxidation of cyclic 1,3-dienes catalyzed by a sterically and electronically optimized (salen)Mn complex

Chang, Sukbok,Heid, Richard M.,Jacobsen, Eric N.

, p. 669 - 672 (2007/10/02)

Chiral (salen)Mn(III)Cl complexes catalyze epoxidation of cyclic 1,3-dienes with moderate-to-good enantioselectivity. A new catalyst (2), bearing sterically hindered and electron donating (OSi(iPr)3 (OTIPS) substituents, induces up to 12% higher selectivity than the previously-reported tert-butyl substituted analog 1.

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