19718-45-7 Usage
General Description
2-Naphthyl propyl ether, also known as 2-naphthalenemethanol propyl ether, is a carbon-based organic compound. This chemical is an ether due to the presence of an oxygen atom connected to two alkyl or aryl groups - in this case, a 2-naphthyl group and a propyl group. The compound is commonly used in the synthesis of other compounds due to its ether linkage which is quite stable and generally unreactive. Its stability and usefulness in synthesis make it an important chemical in industrial applications. It is also an aromatic compound due to the presence of a naphthalene ring, which can make it potentially hazardous due to possible bioaccumulation and persistence in the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 19718-45-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,1 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19718-45:
(7*1)+(6*9)+(5*7)+(4*1)+(3*8)+(2*4)+(1*5)=137
137 % 10 = 7
So 19718-45-7 is a valid CAS Registry Number.
19718-45-7Relevant articles and documents
A Simple One-step Synthesis of Phenyl Ethers from Phenyl Acetates
Banerjee, Sunil K.,Gupta, Bishan D.,Singh, Kuber
, p. 815 - 816 (1982)
Phenyl acetates when refluxed with alkyl halides in acetone solution in the presence of a crown ether and anhydrous potassium carbonate undergo alkylation yielding phenyl ethers.
Synthesis of regioisomeric naphtho-furans via naphthyloxyalkanals
Kwiecien,Witczak,Kowalewska,Augustyniak
experimental part, p. 20 - 29 (2010/08/06)
A new route to the regioisomeric 2-alkylnaphtho[2,1-b]- and 2-alkylnaphtho[1,2-b]furans via acid-catalyzed cyclization of the corresponding 2-naphthyloxyalkanals under mild conditions over Amberlyst 15 resin has been described. The 2-naphthyloxyalkanals w
Acylation of naphthalenes
-
, (2008/06/13)
Naphthalene substituted in the 2- or β-position with an electron-donating substituent can be acylated with high regioselectivity in the 6-position by using an acylating agent in substantially anhydrous hydrogen fluoride which functions both as catalyst and solvent.
