10275-58-8 Usage
Description
2,7-Di-tert-butyl naphthalene, with the molecular formula C22H28, is a polycyclic aromatic hydrocarbon derived from naphthalene. This chemical compound features two tert-butyl groups attached to the 2 and 7 positions of the naphthalene ring, endowing it with high thermal stability, a high boiling point, and resistance to oxidation. These properties make it a valuable chemical in various manufacturing processes.
Uses
Used in Heat Transfer and Lubrication Industry:
2,7-Di-tert-butyl naphthalene is used as a heat transfer and lubricating fluid due to its high thermal stability, which allows it to maintain its properties under high-temperature conditions without breaking down.
Used in Plastics, Coatings, and Rubber Industry:
In the plastics, coatings, and rubber industry, 2,7-Di-tert-butyl naphthalene serves as a photostabilizer to protect products from damaging UV radiation, thereby enhancing their durability and longevity.
Used in Chemical Synthesis:
2,7-Di-tert-butyl naphthalene is utilized as a chemical intermediate in the synthesis of other organic compounds, contributing to the creation of a wide range of chemical products.
Used in Manufacturing Processes:
Due to its high boiling point and resistance to oxidation, 2,7-Di-tert-butyl naphthalene is a valuable component in numerous manufacturing processes, where it plays a crucial role in the production of various industrial and consumer goods.
Check Digit Verification of cas no
The CAS Registry Mumber 10275-58-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,7 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10275-58:
(7*1)+(6*0)+(5*2)+(4*7)+(3*5)+(2*5)+(1*8)=78
78 % 10 = 8
So 10275-58-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H24/c1-17(2,3)15-9-7-13-8-10-16(18(4,5)6)12-14(13)11-15/h7-12H,1-6H3
10275-58-8Relevant articles and documents
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Whitmore,James
, p. 2088 (1943)
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Crawford,Glesmann
, p. 1108 (1954)
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Fieser,Price
, p. 1838,1841 (1936)
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Price et al.
, p. 517,519 (1942)
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The alkylation of naphthalene over one-dimensional twelve-membered ring zeolites. the influence of zeolite structure and alkylating agent on the selectivity for dialkylnaphthalenes
Sugi, Yoshihiro,Maekawa, Hiroyoshi,Naiki, Hiroaki,Komura, Kenichi,Kubota, Yoshihiro
, p. 897 - 905 (2008)
Alkylation, i.e., isopropylation, s-butylation, and t-butylation, of naphthalene (NP) was examined over one-dimensional twelve-membered (12-MR) zeolites: H-mordenite (MOR), SSZ-24 (AFI), SSZ-55 (ATS), and SSZ-42 (IFR) in order to elucidate how zeolite str
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Contractor,Peters,Rowe
, p. 1993,1995 (1949)
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The alkylation of naphthalene over one-dimensional fourteen-membered ring zeolites. the influence of zeolite structure and alkylating agent on the selectivity for dialkylnaphthalenes
Sugi, Yoshihiro,Maekawa, Hiroyoshi,Naiki, Hiroaki,Komura, Kenichi,Kubota, Yoshihiro
experimental part, p. 1166 - 1174 (2009/05/06)
The alkylation, i.e., isopropylation, s-butylation, and t-butylation, of naphthalene (NP) was examined over one-dimensional fourteen-membered (14-MR) zeolites: CIT-5 (CF1), UTD-1 (DON), and SSZ-53 (SFH), and compared to the results over H-mordenite (MOR)
