2173-57-1 Usage
Description
β-Naphthyl isobutyl ether has a sweet, fruity, delicately neroli- orange blossom floral odor. This substance may be prepared by simple etherification of naphthol with a surplus of isobutanol under reflux in the presence of sulfuric acid.
Chemical Properties
Different sources of media describe the Chemical Properties of 2173-57-1 differently. You can refer to the following data:
1. β-Naphthyl isobutyl ether has a sweet, fruity, delicately neroli-orange blossom, floral odor
2. Isobutyl 2-Naphthyl Ether forms white crystals (mp 33–33.5°C)
with a fruity, orange blossom odor.
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.
