2173-57-1 Usage
Description
2-Isobutoxynaphthalene, also known as β-Naphthyl isobutyl ether or Isobutyl 2-Naphthyl Ether, is an organic compound with a sweet, fruity, and delicately neroli-orange blossom floral odor. It is prepared through a simple etherification process of naphthol with a surplus of isobutanol under reflux in the presence of sulfuric acid. This substance forms white crystals with a melting point of 33-33.5°C.
Uses
Used in Fragrance Industry:
2-Isobutoxynaphthalene is used as a fragrance ingredient for its sweet, fruity, and delicately neroli-orange blossom floral odor. It is particularly suitable for creating a pleasant and long-lasting scent in various perfumes, colognes, and other fragrance products.
Used in Flavor Industry:
In the flavor industry, 2-Isobutoxynaphthalene is used as an additive to enhance the taste and aroma of various food and beverage products. Its sweet and fruity characteristics make it an ideal choice for creating unique and appealing flavors in the culinary world.
Used in Chemical Synthesis:
2-Isobutoxynaphthalene can also be used as a starting material or intermediate in the synthesis of various organic compounds, including pharmaceuticals, dyes, and other specialty chemicals. Its unique chemical structure allows for further functionalization and modification to create a wide range of products with diverse applications.
Preparation
By simple etherification of naphthol with a surplus of isobutanol under reflux in the presence of sulfuric acid.
Flammability and Explosibility
Notclassified
Check Digit Verification of cas no
The CAS Registry Mumber 2173-57-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,7 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2173-57:
(6*2)+(5*1)+(4*7)+(3*3)+(2*5)+(1*7)=71
71 % 10 = 1
So 2173-57-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H16O/c1-11(2)10-15-14-8-7-12-5-3-4-6-13(12)9-14/h3-9,11H,10H2,1-2H3
2173-57-1Relevant articles and documents
Reduced Phenalenyl in Catalytic Dehalogenative Deuteration and Hydrodehalogenation of Aryl Halides
Singh, Bhagat,Ahmed, Jasimuddin,Biswas, Amit,Paira, Rupankar,Mandal, Swadhin K.
, p. 7242 - 7255 (2021/05/29)
Dehalogenative deuteration reactions are generally performed through metal-mediated processes. This report demonstrates a mild protocol for hydrodehalogenation and dehalogenative deuteration of aryl/heteroaryl halides (39 examples) using a reduced odd alternant hydrocarbon phenalenyl under transition metal-free conditions and has been employed successfully for the incorporation of deuterium in various biologically active compounds. The combined approach of experimental and theoretical studies revealed a single electron transfer-based mechanism.
Methylation of arenes via Ni-catalyzed aryl C-O/F activation
Guan, Bing-Tao,Xiang, Shi-Kai,Wu, Tao,Sun, Zuo-Peng,Wang, Bi-Qin,Zhao, Ke-Qing,Shi, Zhang-Jie
, p. 1437 - 1439 (2008/12/21)
Aryl C-O and C-F can be transformed into C-Me via Ni-catalyzed coupling with MeMgBr under mild conditions. The Royal Society of Chemistry.
